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Roxee Meds Catalog

Oxytetracycline

Medication catalog facts with explicit FDA-approval, off-label, source-limited, and safety context.

Both Catalog complete FDA data linked Rx required Liquid (Solution) Multiple FDA labelers Official label facts Owner quick guide first

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Data freshness

Storefront facts
Catalog refreshed
May 5, 2026, 10:00 a.m.

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FDA applications
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Sponsor, product, and application records imported from Animal Drugs @ FDA.

Safety reports
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openFDA reaction terms and case summaries are supporting evidence, not proof of causality.

Source timing details
Source timing details
  • Storefront facts: Source Roxee | Refreshed May 5, 2026, 10:00 AM UTC
    The storefront fact projection used for browse cards and quick facts.
  • Animal Drugs @ FDA: Source FDA | Refreshed May 5, 2026, 10:00 AM UTC
    Applications/products are imported from FDA export data.
  • Animal Drugs @ FDA previews: Source FDA | Refreshed Mar 13, 2026, 10:01 AM UTC
    Label highlights/doc links are fetched from FDA preview endpoints.
  • Animal Drug Product Listing Directory (NDC): Source FDA | Refreshed May 5, 2026, 10:00 AM UTC
    Package/product NDCs from FDA’s electronic listing directory (XLS).

Evidence

Reviewed / Updated / Sources

Reviewed by: Not available

Last reviewed: February 12, 2026

Updated: February 12, 2026, 10:44 PM UTC

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Oxytetracycline

Oxytetracycline

Drug type: Generic ingredient • Branded profile FDA branded products available

Both Liquid (Solution) Rx required 100% storefront ready

Species: Both

Manufacturer: Multiple FDA labelers

Medication Snapshot

Merged from the current Roxee medication system with field-level provenance, freshness, and completeness tracking.

Oxytetracycline

It is used in dogs for the treatment of bacterial pneumonia caused by Brucella bronchiseptica, tonsillitis caused by Streptococcus hemolyticus, bacterial enteritis caused by Escherichia coli, urinary tract infections caused by Escherichia coli, and wound infections caused by Staphylococcus aureus. The drug can be used for continuation of compatible antibiotic therapy following parenteral oxytetracycline administration where rapidly attained, sustained antibiotic blood levels are required. The duration of treatment required to obtain favorable response will depend to some extent on the severity and degree of involvement and the susceptibility of the infectious agent. Clinical response to antibiotic therapy usually occurs within 48 to 72 hours. If improvement is not observed within that period, the diagnosis and course of treatment should be reconsidered. To assure adequate treatment, administration of the drug should continue for at least 48 hours following favorable clinical response. It is used in cats for the treatment of bacterial pneumonia caused by Brucella bronchiseptica, tonsillitis caused by Streptococcus hemolyticus, bacterial enteritis caused by Escherichia coli, urinary tract infections caused by Escherichia coli, and wound infections caused by Staphylococcus aureus. The drug can be used for continuation of compatible antibiotic therapy following parenteral oxytetracycline administration where rapidly attained, sustained antibiotic blood levels are required. The duration of treatment required to obtain favorable response will depend to some extent on the severity and degree of involvement and the susceptibility of the infectious agent. Clinical response to antibiotic therapy usually occurs within 48 to 72 hours. If improvement is not observed within that period, the diagnosis and course of treatment should be reconsidered. To assure adequate treatment, administration of the drug should continue for at least 48 hours following favorable clinical response. Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline. Species commonly shown: Both, Beef, Calves.

Generic name
Oxytetracycline
Brand names
TM®-10 Premix, Oxyvet-100 Aquachel-100, Terramycin® Premix, Liquamycin® LA-200®
Manufacturer
Multiple FDA labelers
Species
Both, Beef, Calves, Dairy, non-lactating
Dosage forms
Liquid (Solution), Medicated Feed, Injectable Solution, Soluble Powder
Prescription
Prescription required
Completeness
100%
Validation
Complete
Brand names
TM®-10 Premix Oxyvet-100 Aquachel-100 Terramycin® Premix Liquamycin® LA-200® Oxytet® Soluble OXYMarine™ Pennox 50® Pennox 100-MR® Pennox 100 Hi-Flo® Pennox 200 Hi-Flo® Biocyl-50 Biocyl-100 OXY 500 Calf Bolus OXY 1000 Calf Bolus Noromycin® 300 LA Bio-Mycin® 200 Pennox 343® AGRIMYCIN®-343 MAXIM 100 Oxytetracycline Injection MAXIM-200 AGRIMYCIN® 200 Tetroxy® HCA-280 Tetroxy® HCA-1772 Tetroxy® HCA-1400 Tetroxy® 25 Pennox® 200 Geomycin 200 Tetroxy® 343 Oxytetracycline Hydrochloride Soluble Powder Oxytetracycline Injection 200 Oxytet 100 Tetroxy® Aquatic Tetroxy®-LA OXY WS™ Terramycin® 100 for Fish Terramycin® 200 for Fish TERRAMYCIN-343® TERRAMYCIN® TERRAMYCIN® Soluble Powder Concentrate TM-50® TM-50® D TM-100® TM-100®D Terramycin® 10 Terramycin® 30 Terramycin® 50 Terramycin® 100 Terramycin® 200 Terramycin® 200 Granular Terramycin® 100MR OXYJECT® 100 Status™ SQ TM®-5 Antibiotic Feed Supplement Liquamycin® Injectable Terramycin® Injectable Terramycin® Egg Formula Liquimast Solution for Mastitis Terramycin® Scours Tablets Oxyject® OXY-TET 50™ Bio-Mycin® Oxytetracycline-50 Oxy-Tet™ Injection Bio-Mycin C Terramycin® Vet Capsules Terramycin® 100 Liquamycin® 100 Oxytetracycline Premix Purina® Mix-R-Mycin Concentrate Rachelle Oxyvet Injection Medamycin® 100 MEDAMYCIN® Bio-Mycin 200 Tetroxy HCA AGRIMYCIN 200 Noromycin 300 LA TERRA-VET 200 Vetrimycin 200 Liquamycin LA-200 Tetroxy 343 Oxytetracycline Hydrochloride AX Pharmaceutical Corp Terramycin 200 Terramycin 100 MR Terramycin 50 Pennox 50 Pennox 100 Hi-Flo Terramycin 100 Terramycin 200 Granular Oxytet Soluble Oxytetracycline 200 Terramycin Scours Pennox 343 Oxytetracycline HCL Oxytetracycline Dihydrate
Dosage forms
Liquid (Solution) Medicated Feed Injectable Solution Soluble Powder Type A Medicated Article Bolus Solution Powder Powder for solution Tablet Capsule

Indications / Uses

It is used in dogs for the treatment of bacterial pneumonia caused by Brucella bronchiseptica, tonsillitis caused by Streptococcus hemolyticus, bacterial enteritis caused by Escherichia coli, urinary tract infections caused by Escherichia coli, and wound infections caused by Staphylococcus aureus. The drug can be used for continuation of compatible antibiotic therapy following parenteral oxytetracycline administration where rapidly attained, sustained antibiotic blood levels are required. The duration of treatment required to obtain favorable response will depend to some extent on the severity and degree of involvement and the susceptibility of the infectious agent. Clinical response to antibiotic therapy usually occurs within 48 to 72 hours. If improvement is not observed within that period, the diagnosis and course of treatment should be reconsidered. To assure adequate treatment, administration of the drug should continue for at least 48 hours following favorable clinical response. It is used in cats for the treatment of bacterial pneumonia caused by Brucella bronchiseptica, tonsillitis caused by Streptococcus hemolyticus, bacterial enteritis caused by Escherichia coli, urinary tract infections caused by Escherichia coli, and wound infections caused by Staphylococcus aureus. The drug can be used for continuation of compatible antibiotic therapy following parenteral oxytetracycline administration where rapidly attained, sustained antibiotic blood levels are required. The duration of treatment required to obtain favorable response will depend to some extent on the severity and degree of involvement and the susceptibility of the infectious agent. Clinical response to antibiotic therapy usually occurs within 48 to 72 hours. If improvement is not observed within that period, the diagnosis and course of treatment should be reconsidered. To assure adequate treatment, administration of the drug should continue for at least 48 hours following favorable clinical response. Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Warnings / Contraindications

Federal law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption. Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Zero-day slaughter withdrawal in swine.

  • Federal law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption. Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Zero-day slaughter withdrawal in swine.

Side Effects

Top reported reactions (openFDA): Anal sac disorder, Behavioural disorder NOS, Corneal ulcer, Hives (see also 'Skin'), Injection site pain, Leucocytosis NOS.

FAQ

Both, Beef, Calves, Dairy, non-lactating, Chicken, Broilers, No use class stated or implied, Sows, Calves, Including Prerumenative Veal, Dairy, Fish, Finfish, Fry And Fingerlings, Honey Bees, Breeding, Growing, Over 400 Pounds, Broilers, Not laying eggs for human consumption, Excluding turkeys producing eggs for human consumption, Sheep, No Use Class Stated Or Implied, Sows with litters or about to farrow, Dairy, females Under 20 months of age, Growing, Beef and dairy calves, excluding veal calves, Beef And Dairy, Calves including preruminating (veal) calves, Cattle, Dairy, Not Lactating, Swine, No Use Class Stated Or Implied, Swine, Sows With Litters Or About To Farrow, Cattle, Beef, Swine, Breeding Swine, Turkey, Growing, Turkey, Not Laying Eggs For Human Consumption, Chicken, Not Laying Eggs For Human Consumption, Beef And Non-Lactating Dairy, Pacific Salmon, Reared, Freshwater-Reared Salmonids, Catfish, Reared, Freshwater-reared salmonids weighing up to 55 grams, Lobster, Calves, excluding veal calves, Breeders not laying eggs for human consumption, Broilers not laying eggs for human consumption, Beef calves, Dairy calves, Dog, No Use Class Stated Or Implied, Cat, No Use Class Stated Or Implied

Yes. Roxee shows this as prescription-only.

Liquid (Solution), Medicated Feed, Injectable Solution, Soluble Powder

Source Transparency

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Pet Owner Quick Guide

Start here first for the safest next-step summary before the deeper medication detail.

Used for:

For control of infectious synovitis caused by Mycoplasma synoviae ; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosing note:

Exact dosing depends on your pet's species, weight, and health status. Use your veterinarian's instructions for the exact dose and schedule.

What to watch for:

  • Prepare a fresh solution daily
  • Administer 7 to 14 days
  • Not to be used for more than 14 consecutive days
  • Use as sole source of drinking water
  • Do not use in birds producing eggs for human consumption
  • Administer up to 14 days
  • Do not use for more than 14 consecutive days
  • Use as a sole source of oxytetracycline
  • Zero-day slaughter withdrawal in swine
  • Vomiting (1 reports)
  • Urinary bladder disorder NOS (1 reports)
  • very low energy (1 reports)

When to call the vet:

  • Repeated vomiting or diarrhea.
  • Severe lethargy (hard to wake, very low energy).
  • Collapse or fainting.
  • Trouble breathing.
  • Facial swelling or hives.
  • Blood in vomit or stool.

Regulatory restrictions are shown in Vet View.

What to tell or ask your vet today:

  • Is this medicine the right fit for my pet’s current symptoms?
  • Which warning signs mean I should call back right away?
  • How should I handle missed doses or refusal to take the medicine?
Major cautions & emergency warning signs

Side effects to monitor:

  • Prepare a fresh solution daily
  • Administer 7 to 14 days
  • Not to be used for more than 14 consecutive days
  • Use as sole source of drinking water
  • Do not use in birds producing eggs for human consumption

Most reported reactions:

  • Vomiting (1 reports)
  • Urinary bladder disorder NOS (1 reports)
  • Tiredness (lethargy) (1 reports)

Emergency warning signs:

  • Repeated vomiting or diarrhea.
  • Severe lethargy (hard to wake, very low energy).
  • Collapse or fainting.
  • Trouble breathing.

Quick Facts

Official label facts first, then secondary summaries. Marketing content is separated below.

Species: Both
Manufacturer: Multiple FDA labelers
Form: Bolus, Capsule, Injectable Solution, Liquid (Solution), Medicated Feed, Powder
Identifiers:
ANADA: 200008 ANADA: 200026 ANADA: 200066 ANADA: 200068 ANADA: 200096 ANADA: 200117 ANADA: 200123 ANADA: 200128 ANADA: 200144 ANADA: 200146 ANADA: 200154 ANADA: 200232 ANADA: 200247 ANADA: 200305 ANADA: 200306 ANADA: 200452 ANADA: 200460 ANADA: 200537 NADA: 101666 NADA: 103758
Source metadata:

Warnings / Contraindications

Federal law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption. Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Zero-day slaughter withdrawal in swine.

  • High: Federal law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption. Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Zero-day slaughter withdrawal in swine.
Source metadata:

Adverse Reactions

Snapshot first, detailed rows second. This section summarizes signal data and is not a diagnosis.

Tap or hover a reaction to see what it means in plain language.

Tracked signals
32
Reported cases
30
Serious reports
10
Species represented
2
Grouped by Body System
Digestive (3) · Vomiting, Decreased appetite, Loss of appetite Skin & allergy (2) · Hives, Hives (see also 'Skin') Neurologic (3) · Unsteady walking (ataxia), Tiredness (lethargy), Head tilt - neurological disorder Behavior (1) · Behavioral disorder (unspecified) Other (23) · Weight loss, Walking difficulty, Urinary bladder disorder NOS
Most Reported Reactions
Reaction Body system Cases Species Serious cases
Digestive 1 Cat 1
Other 1 Cat 1
Neurologic 1 Cat 1
Other 1 Dog 1
Other 1 Cat 1
Other 1 Dog 1
Other 1 Cat 1
Digestive 1 Cat 1

Species coverage: Cat (19) Dog (13)

View detailed reaction table
Reaction Body system Species Seriousness Frequency Reports
Other Cat Non-serious - 1
Other Cat Non-serious - 1
Digestive Cat Serious - 1
Other Cat Serious - 1
Neurologic Cat Non-serious - 1
Other Cat Non-serious - 1
Neurologic Cat Serious - 1
Other Cat Non-serious - 1
Other Dog Non-serious - 1
Other Dog Non-serious - 1
Other Dog Serious - 1
Other Cat Serious - 1
Other Dog Non-serious - 1
Other Dog Serious - 1
Other Dog Non-serious - 1
Other Dog Non-serious - 1
Other Dog Non-serious - 1
Skin & allergy Dog Non-serious - 1
Neurologic Cat Non-serious - 1
Other Cat Non-serious - 1
Other Cat Non-serious - 1
Other Cat Non-serious - 1
Other Cat Serious - 1
Digestive Cat Serious - 1
Other Cat Serious - 1
Other Dog Non-serious - 1
Other Cat Serious - 1
Behavior Dog Non-serious - 1
Other Dog Non-serious - 1
Other Cat Non-serious - 1
Digestive Cat Unknown - -
Skin & allergy Dog Unknown - -
Source metadata:

Documents

Owner handouts and official technical documents open on-page first, with the original source still one click away.

Owner handouts

0
No owner handouts linked yet.

Official label / PI

8

SPL

100

FOI

67

113-232

Official label / PI · EA

113-232

Official label / PI · FONSI

038-439

Official label / PI · EA

038-439

Official label / PI · FONSI

038-439

Official label / PI · EA

038-439

Official label / PI · FONSI

130-435

Official label / PI · EA

130-435

Official label / PI · FONSI

Pennox 50®

SPL · SPL

FDA Structured Product Label

Pennox 50® Pennox 100-MR® Pennox 100 Hi-Flo® Pennox 200 Hi-Flo®

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Pharmgate Inc.
NADA
138-938
Status
VFD
Form
Type A Medicated Article
Route
Oral
Species
Honey Bees • Breeding • No use class stated or implied • Growing, Over 400 Pounds • Beef • Calves • Dairy, non-lactating • Broilers • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Sheep, No Use Class Stated Or Implied
Composition / specifications
Type A medicated articles contain 50 grams oxytetracycline per pound.

Chickens

Indication

For control of infectious synovitis caused by Mycoplasma synoviae; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

100 to 200 grams per ton of feed. Feed continuously for 7-14 days.

Indication

For control of chronic respiratory disease (CRD) and air sac infection caused by M. gallisepticum and Escherichia coli susceptible to oxytetracycline.

Dosage

400 grams per ton of feed. Feed continuously for 7-14 days.

Broiler chickens

Indication

For reduction of mortality due to air sacculitis (air-sac-infection) caused by E. coli susceptible to oxytetracycline.

Dosage

500 grams per ton of feed. Feed continuously for 5 days.

Turkeys

Indication

For control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.

Dosage

100 grams per ton of feed. Feed continuously for 7 to 14 days.

Indication

For control of infectious synovitis caused by M. synoviae susceptible to oxytetracycline.

Dosage

200 grams per ton of feed. Feed continuously for 7 to 14 days.

Indication

For control of complicating bacterial organisms associated with bluecomb (transmissible enteritis; coronaviral enteritis) susceptible to oxytetracycline.

Dosage

25 milligrams per pound body weight. Feed continuously for 7 to 14 days.

Swine

Indication

For treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis susceptible to oxytetracycline and treatment of bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound body weight daily in feed. Feed continuously for 7 to 14 days.

Swine (breeding)

Indication

For control and treatment of leptospirosis (reducing the incidence of abortion and shedding of leptospirae) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage

10 milligrams per pound body weight daily in feed. Feed continuously for 7 to 14 days.

Cattle (calves, beef, nonlactating dairy)

Indication

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia (shipping fever complex) caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound body weight daily in feed. Feed continuously for 7 to 14 days.

Cattle

Indication

For prevention and treatment of the early stages of shipping fever complex.

Dosage

0.5 to 2.0 grams per head per day in feed. Feed 3 to 5 days before and after arrival in feedlots.

Cattle (growing, over 400 pounds body weight)

Indication

For reduction of the incidence of liver abscesses.

Dosage

75 milligrams per head per day in feed.

Sheep

Indication

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily in feed. Feed continuously for 7 to 14 days.

Honey bees

Indication

For control of American Foulbrood caused by Paenibacillus larvae, and European Foulbrood caused by Streptococcus pluton susceptible to oxytetracycline.

Dosage

200 milligrams / oz dusting of Type C medicated feed per colony every 4 to 5 days for a total of 3 applications

Pennox 100-MR®

SPL · SPL

FDA Structured Product Label

Pennox 50® Pennox 100-MR® Pennox 100 Hi-Flo® Pennox 200 Hi-Flo®

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Pharmgate Inc.
NADA
138-938
Status
VFD
Form
Type A Medicated Article
Route
Oral
Species
Honey Bees • Breeding • No use class stated or implied • Growing, Over 400 Pounds • Beef • Calves • Dairy, non-lactating • Broilers • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Sheep, No Use Class Stated Or Implied
Composition / specifications
Type A medicated articles contain 50 grams oxytetracycline per pound.

Chickens

Indication

For control of infectious synovitis caused by Mycoplasma synoviae; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

100 to 200 grams per ton of feed. Feed continuously for 7-14 days.

Indication

For control of chronic respiratory disease (CRD) and air sac infection caused by M. gallisepticum and Escherichia coli susceptible to oxytetracycline.

Dosage

400 grams per ton of feed. Feed continuously for 7-14 days.

Broiler chickens

Indication

For reduction of mortality due to air sacculitis (air-sac-infection) caused by E. coli susceptible to oxytetracycline.

Dosage

500 grams per ton of feed. Feed continuously for 5 days.

Turkeys

Indication

For control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.

Dosage

100 grams per ton of feed. Feed continuously for 7 to 14 days.

Indication

For control of infectious synovitis caused by M. synoviae susceptible to oxytetracycline.

Dosage

200 grams per ton of feed. Feed continuously for 7 to 14 days.

Indication

For control of complicating bacterial organisms associated with bluecomb (transmissible enteritis; coronaviral enteritis) susceptible to oxytetracycline.

Dosage

25 milligrams per pound body weight. Feed continuously for 7 to 14 days.

Swine

Indication

For treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis susceptible to oxytetracycline and treatment of bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound body weight daily in feed. Feed continuously for 7 to 14 days.

Swine (breeding)

Indication

For control and treatment of leptospirosis (reducing the incidence of abortion and shedding of leptospirae) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage

10 milligrams per pound body weight daily in feed. Feed continuously for 7 to 14 days.

Cattle (calves, beef, nonlactating dairy)

Indication

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia (shipping fever complex) caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound body weight daily in feed. Feed continuously for 7 to 14 days.

Cattle

Indication

For prevention and treatment of the early stages of shipping fever complex.

Dosage

0.5 to 2.0 grams per head per day in feed. Feed 3 to 5 days before and after arrival in feedlots.

Cattle (growing, over 400 pounds body weight)

Indication

For reduction of the incidence of liver abscesses.

Dosage

75 milligrams per head per day in feed.

Sheep

Indication

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily in feed. Feed continuously for 7 to 14 days.

Honey bees

Indication

For control of American Foulbrood caused by Paenibacillus larvae, and European Foulbrood caused by Streptococcus pluton susceptible to oxytetracycline.

Dosage

200 milligrams / oz dusting of Type C medicated feed per colony every 4 to 5 days for a total of 3 applications

Pennox 100 Hi-Flo®

SPL · SPL

FDA Structured Product Label

Pennox 50® Pennox 100-MR® Pennox 100 Hi-Flo® Pennox 200 Hi-Flo®

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Pharmgate Inc.
NADA
138-938
Status
VFD
Form
Type A Medicated Article
Route
Oral
Species
Honey Bees • Breeding • No use class stated or implied • Growing, Over 400 Pounds • Beef • Calves • Dairy, non-lactating • Broilers • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Sheep, No Use Class Stated Or Implied
Composition / specifications
Type A medicated articles contain 50 grams oxytetracycline per pound.

Chickens

Indication

For control of infectious synovitis caused by Mycoplasma synoviae; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

100 to 200 grams per ton of feed. Feed continuously for 7-14 days.

Indication

For control of chronic respiratory disease (CRD) and air sac infection caused by M. gallisepticum and Escherichia coli susceptible to oxytetracycline.

Dosage

400 grams per ton of feed. Feed continuously for 7-14 days.

Broiler chickens

Indication

For reduction of mortality due to air sacculitis (air-sac-infection) caused by E. coli susceptible to oxytetracycline.

Dosage

500 grams per ton of feed. Feed continuously for 5 days.

Turkeys

Indication

For control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.

Dosage

100 grams per ton of feed. Feed continuously for 7 to 14 days.

Indication

For control of infectious synovitis caused by M. synoviae susceptible to oxytetracycline.

Dosage

200 grams per ton of feed. Feed continuously for 7 to 14 days.

Indication

For control of complicating bacterial organisms associated with bluecomb (transmissible enteritis; coronaviral enteritis) susceptible to oxytetracycline.

Dosage

25 milligrams per pound body weight. Feed continuously for 7 to 14 days.

Swine

Indication

For treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis susceptible to oxytetracycline and treatment of bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound body weight daily in feed. Feed continuously for 7 to 14 days.

Swine (breeding)

Indication

For control and treatment of leptospirosis (reducing the incidence of abortion and shedding of leptospirae) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage

10 milligrams per pound body weight daily in feed. Feed continuously for 7 to 14 days.

Cattle (calves, beef, nonlactating dairy)

Indication

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia (shipping fever complex) caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound body weight daily in feed. Feed continuously for 7 to 14 days.

Cattle

Indication

For prevention and treatment of the early stages of shipping fever complex.

Dosage

0.5 to 2.0 grams per head per day in feed. Feed 3 to 5 days before and after arrival in feedlots.

Cattle (growing, over 400 pounds body weight)

Indication

For reduction of the incidence of liver abscesses.

Dosage

75 milligrams per head per day in feed.

Sheep

Indication

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily in feed. Feed continuously for 7 to 14 days.

Honey bees

Indication

For control of American Foulbrood caused by Paenibacillus larvae, and European Foulbrood caused by Streptococcus pluton susceptible to oxytetracycline.

Dosage

200 milligrams / oz dusting of Type C medicated feed per colony every 4 to 5 days for a total of 3 applications

Pennox 200 Hi-Flo®

SPL · SPL

FDA Structured Product Label

Pennox 50® Pennox 100-MR® Pennox 100 Hi-Flo® Pennox 200 Hi-Flo®

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Pharmgate Inc.
NADA
138-938
Status
VFD
Form
Type A Medicated Article
Route
Oral
Species
Honey Bees • Breeding • No use class stated or implied • Growing, Over 400 Pounds • Beef • Calves • Dairy, non-lactating • Broilers • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Sheep, No Use Class Stated Or Implied
Composition / specifications
Type A medicated articles contain 50 grams oxytetracycline per pound.

Chickens

Indication

For control of infectious synovitis caused by Mycoplasma synoviae; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

100 to 200 grams per ton of feed. Feed continuously for 7-14 days.

Indication

For control of chronic respiratory disease (CRD) and air sac infection caused by M. gallisepticum and Escherichia coli susceptible to oxytetracycline.

Dosage

400 grams per ton of feed. Feed continuously for 7-14 days.

Broiler chickens

Indication

For reduction of mortality due to air sacculitis (air-sac-infection) caused by E. coli susceptible to oxytetracycline.

Dosage

500 grams per ton of feed. Feed continuously for 5 days.

Turkeys

Indication

For control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.

Dosage

100 grams per ton of feed. Feed continuously for 7 to 14 days.

Indication

For control of infectious synovitis caused by M. synoviae susceptible to oxytetracycline.

Dosage

200 grams per ton of feed. Feed continuously for 7 to 14 days.

Indication

For control of complicating bacterial organisms associated with bluecomb (transmissible enteritis; coronaviral enteritis) susceptible to oxytetracycline.

Dosage

25 milligrams per pound body weight. Feed continuously for 7 to 14 days.

Swine

Indication

For treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis susceptible to oxytetracycline and treatment of bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound body weight daily in feed. Feed continuously for 7 to 14 days.

Swine (breeding)

Indication

For control and treatment of leptospirosis (reducing the incidence of abortion and shedding of leptospirae) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage

10 milligrams per pound body weight daily in feed. Feed continuously for 7 to 14 days.

Cattle (calves, beef, nonlactating dairy)

Indication

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia (shipping fever complex) caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound body weight daily in feed. Feed continuously for 7 to 14 days.

Cattle

Indication

For prevention and treatment of the early stages of shipping fever complex.

Dosage

0.5 to 2.0 grams per head per day in feed. Feed 3 to 5 days before and after arrival in feedlots.

Cattle (growing, over 400 pounds body weight)

Indication

For reduction of the incidence of liver abscesses.

Dosage

75 milligrams per head per day in feed.

Sheep

Indication

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily in feed. Feed continuously for 7 to 14 days.

Honey bees

Indication

For control of American Foulbrood caused by Paenibacillus larvae, and European Foulbrood caused by Streptococcus pluton susceptible to oxytetracycline.

Dosage

200 milligrams / oz dusting of Type C medicated feed per colony every 4 to 5 days for a total of 3 applications

TERRAMYCIN-343®

SPL · SPL

FDA Structured Product Label

TERRAMYCIN-343® TERRAMYCIN® TERRAMYCIN® Soluble Powder Concentrate

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Phibro Animal Health Corp.
NADA
8622
Status
RX
Form
Powder for solution
Route
Oral, Immersion
Species
Honey Bees • Fish, Finfish, Fry And Fingerlings • Breeding • No use class stated or implied • Beef • Calves • Dairy, females Under 20 months of age • Growing • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Sheep, No Use Class Stated Or Implied
Composition / specifications
Each 1.32 grams of TERRAMYCIN-343® powder contains 1 gram of OTC HCl (packets: 2.39, 4.78, and 9.55 oz.; jars: 2.25 lbs.; and pails: 4.5 lbs.).

Chickens

Indication
Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.
Dosage
200 to 400 milligrams per gallon of drinking water.
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.
Indication

Control of chronic respiratory disease (CRD) and air sac infection caused by Mycoplasma gallisepticum and E. coli susceptible to oxytetracycline; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage
400 to 800 milligrams per gallon of drinking water.
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Turkeys

Indication
Control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.
Dosage
200 - 400 milligrams per gallon of drinking water.
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.
Indication
Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.
Dosage
400 milligrams per gallon of drinking water.
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Turkeys (Growing)

Indication
Control of complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis) susceptible to oxytetracycline.
Dosage
25 milligrams per pound of body weight daily
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Swine

Indication

Control and treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight
Limitations

Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Zero-day slaughter withdrawal in swine.

Breeding Swine

Indication
Control and treatment of leptospirosis (reducing the incidence of abortions and shedding of leptospira) caused by Leptospira Pomona susceptible to oxytetracycline.
Dosage
10 milligrams per pound of body weight
Limitations

Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Zero–day slaughter withdrawal in swine.

Cattle (calves, beef, and non lactating dairy)

Indication

Control and treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight
Limitations
Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as sole source of oxytetracycline. Do not administer this product with milk or milk replacers. Administer 1 hour before or 2 hours after feeding milk or milk replacers. Withdraw 5 days prior to slaughter. A milk discard period has not been established for this product in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older.

Sheep

Indication

Control and treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight
Limitations

Prepare a fresh solution daily. Administer up to 14 days.Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Withdraw 5 days before slaughter.

Honey Bees

Indication

Control and treatment of American foul brood caused by Paenibacillus larvae.

Dosage
200 milligrams per colony, administered via either a 1:1 sugar syrup (equal parts of sugar and water weight to weight) or dusting with a powdered sugar mixture.
Limitations

The drug is administered in 3 applications of sugar syrup or 3 dustings at 4- to 5- day intervals. The drug should be fed early in the spring or fall and consumed by the bees before main honey flow begins to avoid contamination of production honey. Remove at least 6 weeks prior to main honey flow. Dusting of uncapped brood cells has been reported to cause death of larval honey bees. Do not dust uncapped brood cells.

Finfish

Indication
For skeletal marking of finfish fry and fingerlings.
Dosage
Immerse fish in a solution containing 200 to 700 mg oxytetracycline hydrochloride (buffered) per liter of water for 2 to 6 hours.
Limitations
Solution should be tested on a small number of fish before full-scale use. Do not discharge marking immersion water containing oxytetracycline into surface waters. Oxytetracycline HCl will acidify the water. The pH should be maintained at an acceptable level for fish by the addition of a buffer. Monitor water quality and temperature.

TERRAMYCIN®

SPL · SPL

FDA Structured Product Label

TERRAMYCIN-343® TERRAMYCIN® TERRAMYCIN® Soluble Powder Concentrate

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Phibro Animal Health Corp.
NADA
8622
Status
RX
Form
Powder for solution
Route
Oral, Immersion
Species
Honey Bees • Fish, Finfish, Fry And Fingerlings • Breeding • No use class stated or implied • Beef • Calves • Dairy, females Under 20 months of age • Growing • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Sheep, No Use Class Stated Or Implied
Composition / specifications
Each 1.32 grams of TERRAMYCIN-343® powder contains 1 gram of OTC HCl (packets: 2.39, 4.78, and 9.55 oz.; jars: 2.25 lbs.; and pails: 4.5 lbs.).

Chickens

Indication
Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.
Dosage
200 to 400 milligrams per gallon of drinking water.
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.
Indication

Control of chronic respiratory disease (CRD) and air sac infection caused by Mycoplasma gallisepticum and E. coli susceptible to oxytetracycline; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage
400 to 800 milligrams per gallon of drinking water.
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Turkeys

Indication
Control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.
Dosage
200 - 400 milligrams per gallon of drinking water.
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.
Indication
Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.
Dosage
400 milligrams per gallon of drinking water.
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Turkeys (Growing)

Indication
Control of complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis) susceptible to oxytetracycline.
Dosage
25 milligrams per pound of body weight daily
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Swine

Indication

Control and treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight
Limitations

Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Zero-day slaughter withdrawal in swine.

Breeding Swine

Indication
Control and treatment of leptospirosis (reducing the incidence of abortions and shedding of leptospira) caused by Leptospira Pomona susceptible to oxytetracycline.
Dosage
10 milligrams per pound of body weight
Limitations

Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Zero–day slaughter withdrawal in swine.

Cattle (calves, beef, and non lactating dairy)

Indication

Control and treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight
Limitations
Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as sole source of oxytetracycline. Do not administer this product with milk or milk replacers. Administer 1 hour before or 2 hours after feeding milk or milk replacers. Withdraw 5 days prior to slaughter. A milk discard period has not been established for this product in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older.

Sheep

Indication

Control and treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight
Limitations

Prepare a fresh solution daily. Administer up to 14 days.Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Withdraw 5 days before slaughter.

Honey Bees

Indication

Control and treatment of American foul brood caused by Paenibacillus larvae.

Dosage
200 milligrams per colony, administered via either a 1:1 sugar syrup (equal parts of sugar and water weight to weight) or dusting with a powdered sugar mixture.
Limitations

The drug is administered in 3 applications of sugar syrup or 3 dustings at 4- to 5- day intervals. The drug should be fed early in the spring or fall and consumed by the bees before main honey flow begins to avoid contamination of production honey. Remove at least 6 weeks prior to main honey flow. Dusting of uncapped brood cells has been reported to cause death of larval honey bees. Do not dust uncapped brood cells.

Finfish

Indication
For skeletal marking of finfish fry and fingerlings.
Dosage
Immerse fish in a solution containing 200 to 700 mg oxytetracycline hydrochloride (buffered) per liter of water for 2 to 6 hours.
Limitations
Solution should be tested on a small number of fish before full-scale use. Do not discharge marking immersion water containing oxytetracycline into surface waters. Oxytetracycline HCl will acidify the water. The pH should be maintained at an acceptable level for fish by the addition of a buffer. Monitor water quality and temperature.

TERRAMYCIN® Soluble Powder Concentrate

SPL · SPL

FDA Structured Product Label

TERRAMYCIN-343® TERRAMYCIN® TERRAMYCIN® Soluble Powder Concentrate

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Phibro Animal Health Corp.
NADA
8622
Status
RX
Form
Powder for solution
Route
Oral, Immersion
Species
Honey Bees • Fish, Finfish, Fry And Fingerlings • Breeding • No use class stated or implied • Beef • Calves • Dairy, females Under 20 months of age • Growing • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Sheep, No Use Class Stated Or Implied
Composition / specifications
Each 1.32 grams of TERRAMYCIN-343® powder contains 1 gram of OTC HCl (packets: 2.39, 4.78, and 9.55 oz.; jars: 2.25 lbs.; and pails: 4.5 lbs.).

Chickens

Indication
Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.
Dosage
200 to 400 milligrams per gallon of drinking water.
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.
Indication

Control of chronic respiratory disease (CRD) and air sac infection caused by Mycoplasma gallisepticum and E. coli susceptible to oxytetracycline; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage
400 to 800 milligrams per gallon of drinking water.
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Turkeys

Indication
Control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.
Dosage
200 - 400 milligrams per gallon of drinking water.
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.
Indication
Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.
Dosage
400 milligrams per gallon of drinking water.
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Turkeys (Growing)

Indication
Control of complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis) susceptible to oxytetracycline.
Dosage
25 milligrams per pound of body weight daily
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Swine

Indication

Control and treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight
Limitations

Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Zero-day slaughter withdrawal in swine.

Breeding Swine

Indication
Control and treatment of leptospirosis (reducing the incidence of abortions and shedding of leptospira) caused by Leptospira Pomona susceptible to oxytetracycline.
Dosage
10 milligrams per pound of body weight
Limitations

Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Zero–day slaughter withdrawal in swine.

Cattle (calves, beef, and non lactating dairy)

Indication

Control and treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight
Limitations
Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as sole source of oxytetracycline. Do not administer this product with milk or milk replacers. Administer 1 hour before or 2 hours after feeding milk or milk replacers. Withdraw 5 days prior to slaughter. A milk discard period has not been established for this product in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older.

Sheep

Indication

Control and treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight
Limitations

Prepare a fresh solution daily. Administer up to 14 days.Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Withdraw 5 days before slaughter.

Honey Bees

Indication

Control and treatment of American foul brood caused by Paenibacillus larvae.

Dosage
200 milligrams per colony, administered via either a 1:1 sugar syrup (equal parts of sugar and water weight to weight) or dusting with a powdered sugar mixture.
Limitations

The drug is administered in 3 applications of sugar syrup or 3 dustings at 4- to 5- day intervals. The drug should be fed early in the spring or fall and consumed by the bees before main honey flow begins to avoid contamination of production honey. Remove at least 6 weeks prior to main honey flow. Dusting of uncapped brood cells has been reported to cause death of larval honey bees. Do not dust uncapped brood cells.

Finfish

Indication
For skeletal marking of finfish fry and fingerlings.
Dosage
Immerse fish in a solution containing 200 to 700 mg oxytetracycline hydrochloride (buffered) per liter of water for 2 to 6 hours.
Limitations
Solution should be tested on a small number of fish before full-scale use. Do not discharge marking immersion water containing oxytetracycline into surface waters. Oxytetracycline HCl will acidify the water. The pH should be maintained at an acceptable level for fish by the addition of a buffer. Monitor water quality and temperature.

Terramycin® 10

SPL · SPL

FDA Structured Product Label

Terramycin® 10 Terramycin® 30 Terramycin® 50 Terramycin® 100 Terramycin® 200 Terramycin® 200 Granular Terramycin® 100MR

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Phibro Animal Health Corp.
NADA
95143
Status
VFD
Form
Type A Medicated Article
Route
Oral
Species
Honey Bees • Breeding • No use class stated or implied • Beef • Calves • Dairy, non-lactating • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Sheep, No Use Class Stated Or Implied
Composition / specifications
Type A medicated articles contain 10 grams oxytetracycline per pound.

Chickens

Indication

For control of infectious synovitis caused by Mycoplasma synoviae; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

100 to 200 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. At 500 g/ton level,withdraw 24 hours before slaughter. Zero-day withdrawal period for lower use levels. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues. Do not administer to chickens producing eggs for human consumption.

Indication

For control of chronic respiratory disease (CRD) and air sac infection caused by Mycoplasma gallisepticum and Escherichia coli susceptible to oxytetracycline.

Dosage

400 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. At 500 g/ton level, withdraw 24 hours before slaughter. Zero-day withdrawal period for lower use levels. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues. Do not administer to chickens producing eggs for human consumption.

Indication

For reduction of mortality due to air sacculitis (air-sac-infection) caused by Escherichia coli susceptible to oxytetracycline.

Dosage

500 grams per ton of feed.

Limitations

Feed continuously for 5 days. At 500 g/ton level, withdraw 24 hours before slaughter. Zero-day withdrawal period for lower use levels. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues. Do not administer to chickens producing eggs for human consumption.

Turkeys

Indication

For control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.

Dosage

100 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. Do not administer to turkeys producing eggs for human consumption.

Indication

For control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage

200 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not administer to turkeys producing eggs for human consumption.

Indication

For control of complicating bacterial organisms associated with bluecomb (transmissible enteritis; coronaviral enteritis) susceptible to oxytetracycline.

Dosage

25 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not administer to turkeys producing eggs for human consumption.

Swine

Indication

For treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis susceptible to oxytetracycline and treatment of bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days.

Swine (breeding)

Indication

For control and treatment of leptospirosis (reducing the incidence of abortion and shedding of leptospirae) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 14 days.

Cattle (calves, beef, and nonlactating dairy)

Indication

For growing cattle (over 400 lb) for the reduction of the incidence of liver abscesses.

Dosage

75 milligrams per head per day.

Limitations

Feed continuously.

Indication

For prevention and treatment of the early stages of shipping fever complex.

Dosage

0.5 to 2.0 grams per head per day.

Limitations

Feed 3 to 5 days before and after arrival in feedlots.

Indication

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia (shipping fever complex) caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Zero-day withdrawal time.

Cattle (calves)

Indication

For treatment of bacterial enteritis caused by Escherichia coli susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days in milk replacer or starter feed. Zero-day withdrawal time.

Sheep

Indication

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Withdrawal 5 days before slaughter.

Honey bees

Indication

For control of American Foulbrood caused by Paenibacillus larvae, and European Foulbrood caused by Streptococcus pluton susceptible to oxytetracycline.

Dosage

200 milligrams per colony.

Limitations

Remove at least 6 weeks prior to main honey flow.

Terramycin® 30

SPL · SPL

FDA Structured Product Label

Terramycin® 10 Terramycin® 30 Terramycin® 50 Terramycin® 100 Terramycin® 200 Terramycin® 200 Granular Terramycin® 100MR

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Phibro Animal Health Corp.
NADA
95143
Status
VFD
Form
Type A Medicated Article
Route
Oral
Species
Honey Bees • Breeding • No use class stated or implied • Beef • Calves • Dairy, non-lactating • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Sheep, No Use Class Stated Or Implied
Composition / specifications
Type A medicated articles contain 10 grams oxytetracycline per pound.

Chickens

Indication

For control of infectious synovitis caused by Mycoplasma synoviae; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

100 to 200 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. At 500 g/ton level,withdraw 24 hours before slaughter. Zero-day withdrawal period for lower use levels. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues. Do not administer to chickens producing eggs for human consumption.

Indication

For control of chronic respiratory disease (CRD) and air sac infection caused by Mycoplasma gallisepticum and Escherichia coli susceptible to oxytetracycline.

Dosage

400 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. At 500 g/ton level, withdraw 24 hours before slaughter. Zero-day withdrawal period for lower use levels. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues. Do not administer to chickens producing eggs for human consumption.

Indication

For reduction of mortality due to air sacculitis (air-sac-infection) caused by Escherichia coli susceptible to oxytetracycline.

Dosage

500 grams per ton of feed.

Limitations

Feed continuously for 5 days. At 500 g/ton level, withdraw 24 hours before slaughter. Zero-day withdrawal period for lower use levels. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues. Do not administer to chickens producing eggs for human consumption.

Turkeys

Indication

For control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.

Dosage

100 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. Do not administer to turkeys producing eggs for human consumption.

Indication

For control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage

200 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not administer to turkeys producing eggs for human consumption.

Indication

For control of complicating bacterial organisms associated with bluecomb (transmissible enteritis; coronaviral enteritis) susceptible to oxytetracycline.

Dosage

25 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not administer to turkeys producing eggs for human consumption.

Swine

Indication

For treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis susceptible to oxytetracycline and treatment of bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days.

Swine (breeding)

Indication

For control and treatment of leptospirosis (reducing the incidence of abortion and shedding of leptospirae) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 14 days.

Cattle (calves, beef, and nonlactating dairy)

Indication

For growing cattle (over 400 lb) for the reduction of the incidence of liver abscesses.

Dosage

75 milligrams per head per day.

Limitations

Feed continuously.

Indication

For prevention and treatment of the early stages of shipping fever complex.

Dosage

0.5 to 2.0 grams per head per day.

Limitations

Feed 3 to 5 days before and after arrival in feedlots.

Indication

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia (shipping fever complex) caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Zero-day withdrawal time.

Cattle (calves)

Indication

For treatment of bacterial enteritis caused by Escherichia coli susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days in milk replacer or starter feed. Zero-day withdrawal time.

Sheep

Indication

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Withdrawal 5 days before slaughter.

Honey bees

Indication

For control of American Foulbrood caused by Paenibacillus larvae, and European Foulbrood caused by Streptococcus pluton susceptible to oxytetracycline.

Dosage

200 milligrams per colony.

Limitations

Remove at least 6 weeks prior to main honey flow.

Terramycin® 50

SPL · SPL

FDA Structured Product Label

Terramycin® 10 Terramycin® 30 Terramycin® 50 Terramycin® 100 Terramycin® 200 Terramycin® 200 Granular Terramycin® 100MR

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Phibro Animal Health Corp.
NADA
95143
Status
VFD
Form
Type A Medicated Article
Route
Oral
Species
Honey Bees • Breeding • No use class stated or implied • Beef • Calves • Dairy, non-lactating • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Sheep, No Use Class Stated Or Implied
Composition / specifications
Type A medicated articles contain 10 grams oxytetracycline per pound.

Chickens

Indication

For control of infectious synovitis caused by Mycoplasma synoviae; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

100 to 200 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. At 500 g/ton level,withdraw 24 hours before slaughter. Zero-day withdrawal period for lower use levels. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues. Do not administer to chickens producing eggs for human consumption.

Indication

For control of chronic respiratory disease (CRD) and air sac infection caused by Mycoplasma gallisepticum and Escherichia coli susceptible to oxytetracycline.

Dosage

400 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. At 500 g/ton level, withdraw 24 hours before slaughter. Zero-day withdrawal period for lower use levels. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues. Do not administer to chickens producing eggs for human consumption.

Indication

For reduction of mortality due to air sacculitis (air-sac-infection) caused by Escherichia coli susceptible to oxytetracycline.

Dosage

500 grams per ton of feed.

Limitations

Feed continuously for 5 days. At 500 g/ton level, withdraw 24 hours before slaughter. Zero-day withdrawal period for lower use levels. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues. Do not administer to chickens producing eggs for human consumption.

Turkeys

Indication

For control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.

Dosage

100 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. Do not administer to turkeys producing eggs for human consumption.

Indication

For control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage

200 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not administer to turkeys producing eggs for human consumption.

Indication

For control of complicating bacterial organisms associated with bluecomb (transmissible enteritis; coronaviral enteritis) susceptible to oxytetracycline.

Dosage

25 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not administer to turkeys producing eggs for human consumption.

Swine

Indication

For treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis susceptible to oxytetracycline and treatment of bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days.

Swine (breeding)

Indication

For control and treatment of leptospirosis (reducing the incidence of abortion and shedding of leptospirae) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 14 days.

Cattle (calves, beef, and nonlactating dairy)

Indication

For growing cattle (over 400 lb) for the reduction of the incidence of liver abscesses.

Dosage

75 milligrams per head per day.

Limitations

Feed continuously.

Indication

For prevention and treatment of the early stages of shipping fever complex.

Dosage

0.5 to 2.0 grams per head per day.

Limitations

Feed 3 to 5 days before and after arrival in feedlots.

Indication

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia (shipping fever complex) caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Zero-day withdrawal time.

Cattle (calves)

Indication

For treatment of bacterial enteritis caused by Escherichia coli susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days in milk replacer or starter feed. Zero-day withdrawal time.

Sheep

Indication

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Withdrawal 5 days before slaughter.

Honey bees

Indication

For control of American Foulbrood caused by Paenibacillus larvae, and European Foulbrood caused by Streptococcus pluton susceptible to oxytetracycline.

Dosage

200 milligrams per colony.

Limitations

Remove at least 6 weeks prior to main honey flow.

Terramycin® 100

SPL · SPL

FDA Structured Product Label

Terramycin® 10 Terramycin® 30 Terramycin® 50 Terramycin® 100 Terramycin® 200 Terramycin® 200 Granular Terramycin® 100MR

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Phibro Animal Health Corp.
NADA
95143
Status
VFD
Form
Type A Medicated Article
Route
Oral
Species
Honey Bees • Breeding • No use class stated or implied • Beef • Calves • Dairy, non-lactating • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Sheep, No Use Class Stated Or Implied
Composition / specifications
Type A medicated articles contain 10 grams oxytetracycline per pound.

Chickens

Indication

For control of infectious synovitis caused by Mycoplasma synoviae; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

100 to 200 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. At 500 g/ton level,withdraw 24 hours before slaughter. Zero-day withdrawal period for lower use levels. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues. Do not administer to chickens producing eggs for human consumption.

Indication

For control of chronic respiratory disease (CRD) and air sac infection caused by Mycoplasma gallisepticum and Escherichia coli susceptible to oxytetracycline.

Dosage

400 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. At 500 g/ton level, withdraw 24 hours before slaughter. Zero-day withdrawal period for lower use levels. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues. Do not administer to chickens producing eggs for human consumption.

Indication

For reduction of mortality due to air sacculitis (air-sac-infection) caused by Escherichia coli susceptible to oxytetracycline.

Dosage

500 grams per ton of feed.

Limitations

Feed continuously for 5 days. At 500 g/ton level, withdraw 24 hours before slaughter. Zero-day withdrawal period for lower use levels. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues. Do not administer to chickens producing eggs for human consumption.

Turkeys

Indication

For control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.

Dosage

100 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. Do not administer to turkeys producing eggs for human consumption.

Indication

For control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage

200 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not administer to turkeys producing eggs for human consumption.

Indication

For control of complicating bacterial organisms associated with bluecomb (transmissible enteritis; coronaviral enteritis) susceptible to oxytetracycline.

Dosage

25 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not administer to turkeys producing eggs for human consumption.

Swine

Indication

For treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis susceptible to oxytetracycline and treatment of bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days.

Swine (breeding)

Indication

For control and treatment of leptospirosis (reducing the incidence of abortion and shedding of leptospirae) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 14 days.

Cattle (calves, beef, and nonlactating dairy)

Indication

For growing cattle (over 400 lb) for the reduction of the incidence of liver abscesses.

Dosage

75 milligrams per head per day.

Limitations

Feed continuously.

Indication

For prevention and treatment of the early stages of shipping fever complex.

Dosage

0.5 to 2.0 grams per head per day.

Limitations

Feed 3 to 5 days before and after arrival in feedlots.

Indication

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia (shipping fever complex) caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Zero-day withdrawal time.

Cattle (calves)

Indication

For treatment of bacterial enteritis caused by Escherichia coli susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days in milk replacer or starter feed. Zero-day withdrawal time.

Sheep

Indication

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Withdrawal 5 days before slaughter.

Honey bees

Indication

For control of American Foulbrood caused by Paenibacillus larvae, and European Foulbrood caused by Streptococcus pluton susceptible to oxytetracycline.

Dosage

200 milligrams per colony.

Limitations

Remove at least 6 weeks prior to main honey flow.

Terramycin® 200

SPL · SPL

FDA Structured Product Label

Terramycin® 10 Terramycin® 30 Terramycin® 50 Terramycin® 100 Terramycin® 200 Terramycin® 200 Granular Terramycin® 100MR

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Phibro Animal Health Corp.
NADA
95143
Status
VFD
Form
Type A Medicated Article
Route
Oral
Species
Honey Bees • Breeding • No use class stated or implied • Beef • Calves • Dairy, non-lactating • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Sheep, No Use Class Stated Or Implied
Composition / specifications
Type A medicated articles contain 10 grams oxytetracycline per pound.

Chickens

Indication

For control of infectious synovitis caused by Mycoplasma synoviae; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

100 to 200 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. At 500 g/ton level,withdraw 24 hours before slaughter. Zero-day withdrawal period for lower use levels. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues. Do not administer to chickens producing eggs for human consumption.

Indication

For control of chronic respiratory disease (CRD) and air sac infection caused by Mycoplasma gallisepticum and Escherichia coli susceptible to oxytetracycline.

Dosage

400 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. At 500 g/ton level, withdraw 24 hours before slaughter. Zero-day withdrawal period for lower use levels. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues. Do not administer to chickens producing eggs for human consumption.

Indication

For reduction of mortality due to air sacculitis (air-sac-infection) caused by Escherichia coli susceptible to oxytetracycline.

Dosage

500 grams per ton of feed.

Limitations

Feed continuously for 5 days. At 500 g/ton level, withdraw 24 hours before slaughter. Zero-day withdrawal period for lower use levels. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues. Do not administer to chickens producing eggs for human consumption.

Turkeys

Indication

For control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.

Dosage

100 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. Do not administer to turkeys producing eggs for human consumption.

Indication

For control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage

200 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not administer to turkeys producing eggs for human consumption.

Indication

For control of complicating bacterial organisms associated with bluecomb (transmissible enteritis; coronaviral enteritis) susceptible to oxytetracycline.

Dosage

25 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not administer to turkeys producing eggs for human consumption.

Swine

Indication

For treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis susceptible to oxytetracycline and treatment of bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days.

Swine (breeding)

Indication

For control and treatment of leptospirosis (reducing the incidence of abortion and shedding of leptospirae) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 14 days.

Cattle (calves, beef, and nonlactating dairy)

Indication

For growing cattle (over 400 lb) for the reduction of the incidence of liver abscesses.

Dosage

75 milligrams per head per day.

Limitations

Feed continuously.

Indication

For prevention and treatment of the early stages of shipping fever complex.

Dosage

0.5 to 2.0 grams per head per day.

Limitations

Feed 3 to 5 days before and after arrival in feedlots.

Indication

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia (shipping fever complex) caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Zero-day withdrawal time.

Cattle (calves)

Indication

For treatment of bacterial enteritis caused by Escherichia coli susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days in milk replacer or starter feed. Zero-day withdrawal time.

Sheep

Indication

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Withdrawal 5 days before slaughter.

Honey bees

Indication

For control of American Foulbrood caused by Paenibacillus larvae, and European Foulbrood caused by Streptococcus pluton susceptible to oxytetracycline.

Dosage

200 milligrams per colony.

Limitations

Remove at least 6 weeks prior to main honey flow.

Terramycin® 200 Granular

SPL · SPL

FDA Structured Product Label

Terramycin® 10 Terramycin® 30 Terramycin® 50 Terramycin® 100 Terramycin® 200 Terramycin® 200 Granular Terramycin® 100MR

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Phibro Animal Health Corp.
NADA
95143
Status
VFD
Form
Type A Medicated Article
Route
Oral
Species
Honey Bees • Breeding • No use class stated or implied • Beef • Calves • Dairy, non-lactating • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Sheep, No Use Class Stated Or Implied
Composition / specifications
Type A medicated articles contain 10 grams oxytetracycline per pound.

Chickens

Indication

For control of infectious synovitis caused by Mycoplasma synoviae; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

100 to 200 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. At 500 g/ton level,withdraw 24 hours before slaughter. Zero-day withdrawal period for lower use levels. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues. Do not administer to chickens producing eggs for human consumption.

Indication

For control of chronic respiratory disease (CRD) and air sac infection caused by Mycoplasma gallisepticum and Escherichia coli susceptible to oxytetracycline.

Dosage

400 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. At 500 g/ton level, withdraw 24 hours before slaughter. Zero-day withdrawal period for lower use levels. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues. Do not administer to chickens producing eggs for human consumption.

Indication

For reduction of mortality due to air sacculitis (air-sac-infection) caused by Escherichia coli susceptible to oxytetracycline.

Dosage

500 grams per ton of feed.

Limitations

Feed continuously for 5 days. At 500 g/ton level, withdraw 24 hours before slaughter. Zero-day withdrawal period for lower use levels. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues. Do not administer to chickens producing eggs for human consumption.

Turkeys

Indication

For control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.

Dosage

100 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. Do not administer to turkeys producing eggs for human consumption.

Indication

For control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage

200 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not administer to turkeys producing eggs for human consumption.

Indication

For control of complicating bacterial organisms associated with bluecomb (transmissible enteritis; coronaviral enteritis) susceptible to oxytetracycline.

Dosage

25 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not administer to turkeys producing eggs for human consumption.

Swine

Indication

For treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis susceptible to oxytetracycline and treatment of bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days.

Swine (breeding)

Indication

For control and treatment of leptospirosis (reducing the incidence of abortion and shedding of leptospirae) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 14 days.

Cattle (calves, beef, and nonlactating dairy)

Indication

For growing cattle (over 400 lb) for the reduction of the incidence of liver abscesses.

Dosage

75 milligrams per head per day.

Limitations

Feed continuously.

Indication

For prevention and treatment of the early stages of shipping fever complex.

Dosage

0.5 to 2.0 grams per head per day.

Limitations

Feed 3 to 5 days before and after arrival in feedlots.

Indication

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia (shipping fever complex) caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Zero-day withdrawal time.

Cattle (calves)

Indication

For treatment of bacterial enteritis caused by Escherichia coli susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days in milk replacer or starter feed. Zero-day withdrawal time.

Sheep

Indication

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Withdrawal 5 days before slaughter.

Honey bees

Indication

For control of American Foulbrood caused by Paenibacillus larvae, and European Foulbrood caused by Streptococcus pluton susceptible to oxytetracycline.

Dosage

200 milligrams per colony.

Limitations

Remove at least 6 weeks prior to main honey flow.

Terramycin® 100MR

SPL · SPL

FDA Structured Product Label

Terramycin® 10 Terramycin® 30 Terramycin® 50 Terramycin® 100 Terramycin® 200 Terramycin® 200 Granular Terramycin® 100MR

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Phibro Animal Health Corp.
NADA
95143
Status
VFD
Form
Type A Medicated Article
Route
Oral
Species
Honey Bees • Breeding • No use class stated or implied • Beef • Calves • Dairy, non-lactating • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Sheep, No Use Class Stated Or Implied
Composition / specifications
Type A medicated articles contain 10 grams oxytetracycline per pound.

Chickens

Indication

For control of infectious synovitis caused by Mycoplasma synoviae; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

100 to 200 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. At 500 g/ton level,withdraw 24 hours before slaughter. Zero-day withdrawal period for lower use levels. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues. Do not administer to chickens producing eggs for human consumption.

Indication

For control of chronic respiratory disease (CRD) and air sac infection caused by Mycoplasma gallisepticum and Escherichia coli susceptible to oxytetracycline.

Dosage

400 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. At 500 g/ton level, withdraw 24 hours before slaughter. Zero-day withdrawal period for lower use levels. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues. Do not administer to chickens producing eggs for human consumption.

Indication

For reduction of mortality due to air sacculitis (air-sac-infection) caused by Escherichia coli susceptible to oxytetracycline.

Dosage

500 grams per ton of feed.

Limitations

Feed continuously for 5 days. At 500 g/ton level, withdraw 24 hours before slaughter. Zero-day withdrawal period for lower use levels. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues. Do not administer to chickens producing eggs for human consumption.

Turkeys

Indication

For control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.

Dosage

100 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. Do not administer to turkeys producing eggs for human consumption.

Indication

For control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage

200 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not administer to turkeys producing eggs for human consumption.

Indication

For control of complicating bacterial organisms associated with bluecomb (transmissible enteritis; coronaviral enteritis) susceptible to oxytetracycline.

Dosage

25 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not administer to turkeys producing eggs for human consumption.

Swine

Indication

For treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis susceptible to oxytetracycline and treatment of bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days.

Swine (breeding)

Indication

For control and treatment of leptospirosis (reducing the incidence of abortion and shedding of leptospirae) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 14 days.

Cattle (calves, beef, and nonlactating dairy)

Indication

For growing cattle (over 400 lb) for the reduction of the incidence of liver abscesses.

Dosage

75 milligrams per head per day.

Limitations

Feed continuously.

Indication

For prevention and treatment of the early stages of shipping fever complex.

Dosage

0.5 to 2.0 grams per head per day.

Limitations

Feed 3 to 5 days before and after arrival in feedlots.

Indication

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia (shipping fever complex) caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Zero-day withdrawal time.

Cattle (calves)

Indication

For treatment of bacterial enteritis caused by Escherichia coli susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days in milk replacer or starter feed. Zero-day withdrawal time.

Sheep

Indication

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Withdrawal 5 days before slaughter.

Honey bees

Indication

For control of American Foulbrood caused by Paenibacillus larvae, and European Foulbrood caused by Streptococcus pluton susceptible to oxytetracycline.

Dosage

200 milligrams per colony.

Limitations

Remove at least 6 weeks prior to main honey flow.

Tetroxy®-LA

SPL · SPL

FDA Structured Product Label

Tetroxy®-LA

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Bimeda Animal Health Limited
ANADA
200-537
Status
RX
Form
Injectable Solution
Route
Intramuscular, Intravenous, Subcutaneous
Species
No use class stated or implied • Beef And Dairy • Calves including preruminating (veal) calves
Composition / specifications
200 mg/mL of oxytetracycline base as oxytetracycline dihydrate

Cattle (beef, dairy, and calves including preruminating (veal) calves)

Indication

For the treatment of the following conditions : 1) bacterial pneumonia caused by Pasteurella spp. (shipping fever) in calves and yearlings, where retreatment is impractical due to husbandry conditions, such as cattle on range, or where repeated restraint is inadvisable; 2) infectious bovine keratoconjunctivitis (pinkeye) cause by Moraxella bovis.

Dosage

A single dosage of 9 milligrams per pound of body weight administered by subcutaneous injection.

Indication

For the treatment of pneumonia and shipping fever complex associated with Pasteurella spp. and Haemophilus spp.; infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis; foot rot and diphtheria caused by Fusobacterium necrophorum; bacterial enteritis (scours) caused by Escherichia coli; wooden tongue caused by Actinobacillus lignieresii; leptospirosis caused by Leptospira pomona; and wound infections and acute metritis caused by strains of staphylococci and streptococci organisms sensitive to oxytetracycline.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day, administered by subcutaneous or intravenous injection. In the treatment of severe foot rot and advanced cases of other indicated diseases, a dosage level of 5 milligrams per pound of body weight per day is recommended. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Swine

Indication

For the treatment of bacterial pneumonia caused by Pasteurella multocida, where retreatment is impractical due to husbandry conditions or where repeated restraint is inadvisable.

Dosage

A single dosage of 9 milligrams of per pound of body weight administered intramuscularly.

Indication

For the treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli; pneumonia caused by Pasteurella multocida; and leptospirosis caused by Leptospira pomona.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day administered by intramuscular injection.
Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Sows

Indication

As an aid in the control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.

Dosage

3 mg of oxytetracycline per lb of body weight administered once by intramuscular injection approximately 8 hours before farrowing or immediately after completion of farrowing.

Oxytetracycline Injection

SPL · SPL

FDA Structured Product Label

Oxytetracycline Injection

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Bimeda Animal Health Limited
ANADA
200-117
Status
RX
Form
Injectable Solution
Route
Intravenous, Intramuscular
Species
No use class stated or implied • Sows • Beef • Dairy, non-lactating
Composition / specifications
200 milligrams oxytetracycline per mL

Sows

Indication

As an aid in the control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli

Dosage

3 mg of oxytetracycline per lb of body weight administered once by intramuscular injection approximately 8 hours before farrowing or immediately after completion of farrowing.

Cattle (beef and nonlactating dairy)

Indication

For the treatment of the following conditions : 1) bacterial pneumonia caused by Pasteurella spp. (shipping fever) in yearlings, where re-treatment is impractical due to husbandry conditions, such as cattle on range, or where repeated restraint is inadvisable; 2) infectious bovine keratoconjunctivitis (pinkeye) cause by Moraxella bovis.

Dosage

A single dosage of 9 milligrams per pound of body weight administered intramuscularly. 

Indication

For the treatment of pneumonia and shipping fever complex associated with Pasteurella spp. and Hemophilus spp.; infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis; foot rot and diphtheria caused by Fusobacterium necrophorum; bacterial enteritis (scours) caused by Escherichia coli; wooden tongue caused by Actinobacillus lignieresii; leptospirosis caused by Leptospira pomona; and wound infections and acute metritis caused by strains of staphylococci and streptococci organisms sensitive to oxytetracycline.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day, administered by intravenous or intramuscular injection. In the treatment of severe foot rot and advanced cases of other indicated diseases, a dosage level of 5 milligrams per pound of body weight per day is recommended. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Swine

Indication

For the treatment of bacterial pneumonia caused by Pasteurella multocida, where re-treatment is impractical due to husbandry conditions or where repeated restraint is inadvisable.

Dosage

A single dosage of 9 milligrams of per pound of body weight administered intramuscularly.

Indication

For the treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli; pneumonia caused by Pasteurella multocida; and leptospirosis caused by Leptospira pomona.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day administered by intramuscular injection. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

OXY 500 Calf Bolus

SPL · SPL

FDA Structured Product Label

OXY 500 Calf Bolus OXY 1000 Calf Bolus

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Boehringer Ingelheim Animal Health USA Inc.
NADA
141-002
Status
OTC
Form
Bolus
Route
Oral
Species
Beef • Dairy, non-lactating
Composition / specifications
Each bolus contains 500 or 1000 milligrams of oxytetracycline hydrochloride.

Beef and Dairy Calves

Indication
For control of bacterial enteritis caused by Salmonella typhimurium and Escherichia coli (colibacillosis) and bacterial pneumonia (shipping fever complex, pasteurellosis) caused by Pasteurella multocida.
Dosage
250 milligrams per 100 pounds of body weight every 12 hours (5 milligrams per pound of body weight daily in two doses) for up to four consecutive days.
Limitations
Dosage should continue until the animal returns to normal and for 24 hours to 48 hours after symptoms have subsided. Treatment should not exceed 4 consecutive days. Do not exceed 500 milligrams per 100 pounds of body weight every 12 hours (10 milligrams per pound daily). Discontinue treatment 7 days prior to slaughter. Not for use in lactating dairy cattle. A withdrawal period has not been established for this product in pre-ruminating calves. Do not use in calves to be processed for veal.
Indication
For treatment of bacterial enteritis caused by Salmonella typhimurium and Escherichia coli (colibacillosis) and bacterial pneumonia (shipping fever complex, pasteurellosis) caused by Pasteurella multocida.
Dosage
500 milligrams per 100 pound of body weight every 12 hours (10 milligrams per pound of body weight daily in two doses).
Limitations
Dosage should continue until the animal returns to normal and for 24 hours to 48 hours after symptoms have subsided. Treatment should not exceed 4 consecutive days. Do not exceed 500 milligrams per 100 pounds of body weight every 12 hours (10 milligrams per pound daily). Discontinue treatment 7 days prior to slaughter. Not for use in lactating dairy cattle. A withdrawal period has not been established for this product in pre-ruminating calves. Do not use in calves to be processed for veal.

OXY 1000 Calf Bolus

SPL · SPL

FDA Structured Product Label

OXY 500 Calf Bolus OXY 1000 Calf Bolus

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Boehringer Ingelheim Animal Health USA Inc.
NADA
141-002
Status
OTC
Form
Bolus
Route
Oral
Species
Beef • Dairy, non-lactating
Composition / specifications
Each bolus contains 500 or 1000 milligrams of oxytetracycline hydrochloride.

Beef and Dairy Calves

Indication
For control of bacterial enteritis caused by Salmonella typhimurium and Escherichia coli (colibacillosis) and bacterial pneumonia (shipping fever complex, pasteurellosis) caused by Pasteurella multocida.
Dosage
250 milligrams per 100 pounds of body weight every 12 hours (5 milligrams per pound of body weight daily in two doses) for up to four consecutive days.
Limitations
Dosage should continue until the animal returns to normal and for 24 hours to 48 hours after symptoms have subsided. Treatment should not exceed 4 consecutive days. Do not exceed 500 milligrams per 100 pounds of body weight every 12 hours (10 milligrams per pound daily). Discontinue treatment 7 days prior to slaughter. Not for use in lactating dairy cattle. A withdrawal period has not been established for this product in pre-ruminating calves. Do not use in calves to be processed for veal.
Indication
For treatment of bacterial enteritis caused by Salmonella typhimurium and Escherichia coli (colibacillosis) and bacterial pneumonia (shipping fever complex, pasteurellosis) caused by Pasteurella multocida.
Dosage
500 milligrams per 100 pound of body weight every 12 hours (10 milligrams per pound of body weight daily in two doses).
Limitations
Dosage should continue until the animal returns to normal and for 24 hours to 48 hours after symptoms have subsided. Treatment should not exceed 4 consecutive days. Do not exceed 500 milligrams per 100 pounds of body weight every 12 hours (10 milligrams per pound daily). Discontinue treatment 7 days prior to slaughter. Not for use in lactating dairy cattle. A withdrawal period has not been established for this product in pre-ruminating calves. Do not use in calves to be processed for veal.

AGRIMYCIN® 200

SPL · SPL

FDA Structured Product Label

AGRIMYCIN® 200

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Huvepharma EOOD
ANADA
200-128
Status
RX
Form
Injectable Solution
Route
Intravenous, Subcutaneous, Intramuscular
Species
No use class stated or implied • Sows • Beef And Dairy • Calves including preruminating (veal) calves
Composition / specifications
200 mg oxytetracycline per mL

Beef cattle, dairy cattle, and calves including prerumenative (veal) calves

Indication

For the treatment of the following conditions: 1) bacterial pneumonia caused by Pasteurella spp. (shipping fever) in calves and yearlings, where retreatment is impractical due to husbandry conditions, such as cattle on range, or where repeated restraint is inadvisable; 2) infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis.

Dosage

A single dosage of 9 milligrams oxytetracycline per pound of body weight administered subcutaneously.


Indication

For the treatment of pneumonia and shipping fever complex associated with Pasteurella spp. and Haemophilus spp.; infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis; foot rot and diphtheria caused by Fusobacterium necrophorum; bacterial enteritis (scours) caused by Escherichia coli; wooden tongue caused by Actinobacillus lignieresii; leptospirosis caused by Leptospira pomona; and wound infections and acute metritis caused by strains of staphylococci and streptococci organisms sensitive to oxytetracycline.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day, administered by subcutaneous or intravenous injection. In the treatment of severe foot rot and advanced cases of other indicated diseases, a dosage of 5 milligrams per pound of body weight per day is recommended. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Swine

Indication

For the treatment of bacterial pneumonia caused by Pasteurella multocida, where retreatment is impractical due to husbandry conditions or where repeated restraint is inadvisable.

Dosage

A single dosage of 9 milligrams oxytetracycline per pound of body weight administered intramuscularly.


Indication

For the treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli; pneumonia caused by Pasteurella multocida; and leptospirosis caused by Leptospira pomona.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day administered by intramuscular injection. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Swine (sows)

Indication

As an aid in the control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.

Dosage

3 mg of oxytetracycline per lb of body weight administered once by intramuscular injection approximately 8 hours before farrowing or immediately after completion of farrowing.

Liquamycin® LA-200®

SPL · SPL

FDA Structured Product Label

Liquamycin® LA-200®

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Zoetis Inc.
NADA
113-232
Status
RX
Form
Injectable Solution
Route
Subcutaneous, Intravenous, Intramuscular
Species
No use class stated or implied • Sows • Calves, Including Prerumenative Veal • Beef • Dairy
Composition / specifications
200 mg oxytetracycline base as oxytetracycline dihydrate per mL

Beef cattle, dairy cattle, and calves including prerumenative (veal) calves

Indication

Treatment of infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis; and in the treatment of the following conditions where retreatment is impractical due to husbandry conditions, such as cattle on range, or where their repeated restraint is inadvisable: bacterial pneumonia caused by Pasteurella spp. (shipping fever) in calves and yearlings, and anaplasmosis caused by Anaplasma marginale.

Dosage

A single dosage of 9 milligrams oxytetracycline per pound of body weight administered intramuscularly or subcutaneously.

Indication

For the treatment of pneumonia and shipping fever complex associated with Pasteurella spp. and Hemophilus spp.; infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis; foot rot and diphtheria caused by Fusobacterium necrophorum; bacterial enteritis (scours) caused by Escherichia coli; wooden tongue caused by Actinobacillus lignieresii; leptospirosis caused by Leptospira pomona; anaplasmosis caused by Anaplasma marginale; anthrax caused by Bacillus anthracis; and wound infections and acute metritis caused by strains of staphylococci and streptococci organisms sensitive to oxytetracycline.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day, administered by intravenous, subcutaneous, or intramuscular injection. In the treatment of severe foot-rot and advanced cases of other indicated diseases, a dosage of 5 milligrams per pound of body weight per day is recommended. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Swine

Indication

For the treatment of bacterial pneumonia caused by Pasteurella multocida, where retreatment is impractical due to husbandry conditions or where repeated restraint is inadvisable.

Dosage

A single dosage of 9 milligrams of oxytetracycline per pound of body weight administered intramuscularly.

Indication

For the treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli; pneumonia caused by Pasteurella multocida; and leptospirosis caused by Leptospira pomona.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day administered by intramuscular injection. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Swine (sows)

Indication

As an aid in the control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.

Dosage

3 mg of oxytetracycline per lb of body weight administered once by intramuscular injection approximately 8 hours before farrowing or immediately after completion of farrowing.

Oxytetracycline Injection 200

SPL · SPL

FDA Structured Product Label

Oxytetracycline Injection 200

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Norbrook Laboratories, Ltd.
ANADA
200-306
Status
RX
Form
Injectable Solution
Route
Subcutaneous, Intravenous, Intramuscular
Species
No use class stated or implied • Sows • Beef • Dairy
Composition / specifications
200 mg oxytetracycline per mL

Beef cattle; dairy cattle; and calves, including preruminating (veal) calves

Indication

For the treatment of the following conditions: 1) bacterial pneumonia caused by Pasteurella spp. (shipping fever) in calves and yearlings, where retreatment is impractical due to husbandry conditions, such as cattle on range, or where repeated restraint is inadvisable; 2) infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis.

Dosage

A single dosage of 9 milligrams oxytetracycline per pound of body weight administered intramuscularly or subcutaneously.

Indication

For the treatment of pneumonia and shipping fever complex associated with Pasteurella spp. and Haemophilus spp; infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis; foot rot and diphtheria caused by Fusobacterium necrophorum; bacterial enteritis (scours) caused by Escherichia coli; wooden tongue caused by Actinobacillus lignieresii; leptospirosis caused by Leptospira pomona; and wound infections and acute metritis caused by strains of staphylococci and streptococci organisms sensitive to oxytetracycline.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day, administered by intravenous, subcutaneous, or intramuscular injection. In the treatment of severe foot-rot and advanced cases of other indicated diseases, a dosage of 5 milligrams per pound of body weight per day is recommended. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Swine

Indication

 For the treatment of bacterial pneumonia caused by Pasteurella multocida, where re-treatment is impractical due to husbandry conditions or where repeated restraint is inadvisable.

Dosage

A single dosage of 9 milligrams of oxytetracycline per pound of body weight administered intramuscularly.

Indication

For the treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli; pneumonia caused by Pasteurella multocida; and leptospirosis caused by Leptospira pomona.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day administered by intramuscular injection. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Swine (sows)

Indication

As an aid in the control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.

Dosage

3 mg of oxytetracycline per lb of body weight administered once by intramuscular injection approximately 8 hours before farrowing or immediately after completion of farrowing.

MAXIM-200

SPL · SPL

FDA Structured Product Label

MAXIM-200

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Huvepharma EOOD
ANADA
200-123
Status
RX
Form
Injectable Solution
Route
Subcutaneous, Intravenous, Intramuscular
Species
No use class stated or implied • Sows with litters or about to farrow • Calves, Including Prerumenative Veal • Beef • Dairy
Composition / specifications
200 milligrams oxytetracycline per mL.

Cattle (beef cattle; dairy cattle; calves, including preruminating (veal) calves)

Indication

For the treatment of the following conditions: 1) bacterial pneumonia caused by Pasteurella spp. (shipping fever) in calves and yearlings, where retreatment is impractical due to husbandry conditions, such as cattle on range, or where repeated restraint is inadvisable; 2) infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis.

Dosage

A single dosage of 9 milligrams oxytetracycline per pound of body weight administered intramuscularly or subcutaneously.

Indication

For the treatment of pneumonia and shipping fever complex associated with Pasteurella spp. and Hemophilus spp; infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis; foot-rot and diphtheria caused by Fusobacterium necrophorum; bacterial bacterial enteritis (scours) caused by Escherichia coli; wooden tongue caused by Actinobacillus lignieresii; leptospirosis caused by Leptospira pomona; and wound infections and acute metritis caused by strains of staphylococci and streptococci organisms sensitive to oxytetracycline.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day, administered by intravenous, subcutaneous, or intramuscular injection. In the treatment of severe foot-rot and advanced cases of other indicated diseases, a dosage of 5 milligrams per pound of body weight per day is recommended. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Swine

Indication

Where re-treatment for pneumonia is impractical. For the treatment of bacterial pneumonia caused by Pasteurella multocida, where re-treatment is impractical due to husbandry conditions or where repeated restraint is inadvisable.

Dosage

A single dosage of 9 milligrams oxytetracycline per pound of body weight administered intramuscularly.

Indication

For the treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli; pneumonia caused by Pasteurella multocida; and leptospirosis caused by Leptospira pomona.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day administered by intramuscular injection. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Sows

Indication

As an aid in the control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.

Dosage

3 mg of oxytetracycline per lb of body weight administered once by intramuscular injection approximately 8 hours before farrowing or immediately after completion of farrowing.

Pennox® 200

SPL · SPL

FDA Structured Product Label

Pennox® 200

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Pharmgate Inc.
ANADA
200-154
Status
RX
Form
Injectable Solution
Route
Intravenous, Subcutaneous, Intramuscular
Species
No use class stated or implied • Sows with litters or about to farrow • Beef • Dairy • Calves including preruminating (veal) calves
Composition / specifications
Each mL contains 200 mg of oxytetracycline base as amphoteric oxytetracycline

Cattle (beef cattle; dairy cattle; calves, including preruminating (veal) calves)

Indication

For the treatment of the following conditions: 1) bacterial pneumonia caused by Pasteurella spp. (shipping fever) in calves and yearlings, where retreatment is impractical due to husbandry conditions, such as cattle on range, or where repeated restraint is inadvisable; 2) infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis.

Dosage

A single dosage of 9 milligrams oxytetracycline per pound of body weight administered subcutaneously.

Indication

For the treatment of pneumonia and shipping fever complex associated with Pasteurella spp. and Hemophilus spp.; infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis; foot rot and diphtheria caused by Fusobacterium necrophorum; bacterial enteritis (scours) caused by Escherichia coli; wooden tongue caused by Actinobacillus lignieresii; leptospirosis caused by Leptospira pomona; and wound infections and acute metritis caused by strains of staphylococci and streptococci organisms sensitive to oxytetracycline.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day, administered by subcutaneous or intravenous injection. In the treatment of severe foot rot and advanced cases of other indicated diseases, a dosage of 5 milligrams per pound of body weight per day is recommended. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Swine

Indication

For the treatment of bacterial pneumonia caused by Pasteurella multocida, where retreatment is impractical due to husbandry conditions or where repeated restraint is inadvisable.

Dosage

A single dosage of 9 milligrams oxytetracycline per pound of body weight administered intramuscularly.

Indication

For the treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli; pneumonia caused by Pasteurella multocida; and leptospirosis caused by Leptospira pomona.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day administered by intramuscular injection. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Sows

Indication

As an aid in the control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.

Dosage

3 mg of oxytetracycline per lb of body weight administered once by intramuscular injection approximately 8 hours before farrowing or immediately after completion of farrowing.

MAXIM 100

SPL · SPL

FDA Structured Product Label

MAXIM 100

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Huvepharma EOOD
ANADA
200-068
Status
RX
Form
Injectable Solution
Route
Intravenous
Species
Beef • Dairy, non-lactating • Beef and dairy calves, excluding veal calves
Composition / specifications
Each milliliter of sterile solution contains 100 milligrams of oxytetracycline hydrochloride.

Cattle (beef, non-lactating dairy, and beef and dairy calves [excluding veal])

Indication

Treatment of bacterial pneumonia and shipping fever complex associated with Pasteurella spp.; bacterial enteritis (scours) caused by Escherichia coli; necrotic pododermatitis (foot rot) and calf diphtheria caused by Fusobacterium necrophorum; wooden tongue caused by Actinobacillus lignieresi; and wound infections, acute metritis, and traumatic injury caused by oxytetracycline susceptible staphylococcal and streptococcal organisms.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day (3 to 5 mL per 100 pounds of body weight) by intravenous injection. Severe foot rot and the severe forms of the indicated diseases should be treated with 5 mg per pound of body weight. Treatment should be continued 24 to 48 hours following remission of disease symptoms, not to exceed a total of 4 consecutive days.

Bio-Mycin® 200

SPL · SPL

FDA Structured Product Label

Bio-Mycin® 200

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Boehringer Ingelheim Animal Health USA, Inc.
ANADA
200-008
Status
RX
Form
Injectable Solution
Route
Subcutaneous, Intramuscular, Intravenous
Species
No use class stated or implied • Sows with litters or about to farrow • Beef • Dairy
Composition / specifications
200 milligrams oxytetracycline per milliliter.

Sows

Indication

As an aid in the control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.

Dosage

3 mg of oxytetracycline per lb of body weight administered once by intramuscular injection approximately 8 hours before farrowing or immediately after completion of farrowing.

Cattle (beef and dairy)

Indication

For the treatment of the following conditions : 1) bacterial pneumonia caused by Pasteurella spp. (shipping fever) in yearlings, where re-treatment is impractical due to husbandry conditions, such as cattle on range, or where repeated restraint is inadvisable; 2) infectious bovine keratoconjunctivitis (pinkeye) cause by Moraxella bovis.

Dosage

A single dosage of 9 milligrams per pound of body weight administered intramuscularly or subcutaneously.
Intramuscular administration is not recommended according to Beef Quality Assurance Guidelines.

Indication

For the treatment of pneumonia and shipping fever complex associated with Pasteurella spp. and Haemophilus spp.; infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis; foot-rot and diphtheria caused by Fusobacterium necrophorum; bacterial enteritis (scours) caused by Escherichia coli; wooden tongue caused by Actinobacillus lignieresii; leptospirosis caused by Leptospira pomona; and wound infections and acute metritis caused by strains of staphylococci and streptococci organisms sensitive to oxytetracycline.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day, administered by intravenous, subcutaneous, or intramuscular injection. In the treatment of severe foot rot and advanced cases of other indicated diseases, a dosage level of 5 milligrams per pound of body weight per day is recommended. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment. Intramuscular administration is not recommended according to Beef Quality Assurance Guidelines.

Swine

Indication

For the treatment of bacterial pneumonia caused by Pasteurella multocida, where re-treatment is impractical due to husbandry conditions or where repeated restraint is inadvisable.

Dosage

A single dosage of 9 milligrams of per pound of body weight administered intramuscularly.

Indication

For the treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli; pneumonia caused by Pasteurella multocida; and leptospirosis caused by Leptospira pomona.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day administered by intramuscular injection. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Oxytet 100

SPL · SPL

FDA Structured Product Label

Oxytet 100

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Norbrook Laboratories, Ltd.
ANADA
200-452
Status
RX
Form
Injectable Solution
Route
Intravenous
Species
Beef And Non-Lactating Dairy • Beef and dairy calves, excluding veal calves
Composition / specifications
Each milliliter of sterile solution contains 100 milligrams of oxytetracycline hydrochloride.

Cattle (beef, nonlactating dairy, and beef and dairy calves [excluding veal])

Indication

Treatment of bacterial pneumonia and shipping fever complex associated with Pasteurella spp.; bacterial enteritis (scours) caused by Escherichia coli; necrotic pododermatitis (foot rot) and calf diphtheria caused by Fusobacterium necrophorum; wooden tongue caused by Actinobacillus lignieresi; and wound infections, metritis, and traumatic injury caused by oxytetracycline susceptible staphylococcal and streptococcal organisms.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day (3 to 5 mL per 100 pounds of body weight)
by intravenous injection. Severe foot rot and the severe forms of the indicated diseases should be treated with 5 mg per pound of body weight. Treatment should be continued 24 to 48 hours following remission of disease symptoms, not to exceed a total of 4 consecutive days.

Oxy-Tet™ Injection

SPL · SPL

FDA Structured Product Label

Oxy-Tet™ Injection Bio-Mycin C

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Boehringer Ingelheim Animal Health USA Inc.
NADA
95642
Status
RX/OTC
Form
Liquid (Solution)
Route
Intramuscular
Species
No use class stated or implied • Sows with litters or about to farrow • Beef • Calves • Dairy, non-lactating
Composition / specifications
Each milliliter of sterile solution contains 100 milligrams of oxytetracycline (as oxytetracycline hydrochloride).

Swine

Indication

For treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli, pneumonia caused by Pasteurella multocida, and leptospirosis caused by Leptospira pomona.

Dosage
Three to 5 milligrams of oxytetracycline per pound of body weight per day. Administer intramuscularly.
Limitations
Do not inject more than 5 milliliters per site. Do not use for more than 4 consecutive days. Discontinue treatment at least 26 days before slaughter.

Swine (sows)

Indication

As an aid in control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.

Dosage
3 milligrams of oxytetracycline per pound of body weight, approximately 8 hours before farrowing or immediately after completion of farrowing. Administer intramuscularly.
Limitations
Do not inject more than 5 milliliters per site. Do not use for more than 4 consecutive days. Discontinue treatment at least 26 days before slaughter.

Cattle (beef and nonlactating dairy)

Indication

Treatment of diseases due to oxytetracycline-susceptible organisms as follows: Pneumonia and shipping fever complex associated with Pasteurella species, Hemophilus species, and Klebsiella species, foot-rot and diphtheria caused by Spherophorus necrophorus, bacterial enteritis (scours) caused by Escherichia coli, wooden tongue caused by Actinobacillus lignieresi, leptospirosis caused by Leptospira pomona, and wound infections and acute metritis caused by Staphylococcus species and Streptococcus species. If labeled for use by or on the order of a licensed veterinarian, it may be used for the treatment of anaplasmosis caused by Anaplasma marginale.

Dosage
Three to 5 milligrams of oxytetracycline per pound of body weight per day; 5 milligrams per pound of body weight per day for the treatment of anaplasmosis, severe foot-rot, and severe cases of other indicated diseases. For 100-milligram-per-milliliter solution, administer intramuscularly.
Limitations
Treatment of all diseases should be instituted early and continue for 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 4 consecutive days. Consult your veterinarian if no improvement is noted within 48 hours. Do not inject more than 10 milliliters per site in adult cattle, reducing the volume according to age and body size to 0.5 to 2 milliliters in small calves. Exceeding the highest recommended dose of 5 milligrams per pound of body weight, administering at recommended levels for more than 4 consecutive days, and/or exceeding 10 milliliters intramuscularly per injection site may result in antibiotic residues beyond the withdrawal time. Discontinue treatment at least 18 days prior to slaughter. Not for use in lactating dairy cattle. This drug product is not approved for use in female dairy cattle 20 months of age or older, including dry dairy cows. Use in these cattle may cause drug residues in milk and /or in calves born to these cows.

Bio-Mycin C

SPL · SPL

FDA Structured Product Label

Oxy-Tet™ Injection Bio-Mycin C

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Boehringer Ingelheim Animal Health USA Inc.
NADA
95642
Status
RX/OTC
Form
Liquid (Solution)
Route
Intramuscular
Species
No use class stated or implied • Sows with litters or about to farrow • Beef • Calves • Dairy, non-lactating
Composition / specifications
Each milliliter of sterile solution contains 100 milligrams of oxytetracycline (as oxytetracycline hydrochloride).

Swine

Indication

For treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli, pneumonia caused by Pasteurella multocida, and leptospirosis caused by Leptospira pomona.

Dosage
Three to 5 milligrams of oxytetracycline per pound of body weight per day. Administer intramuscularly.
Limitations
Do not inject more than 5 milliliters per site. Do not use for more than 4 consecutive days. Discontinue treatment at least 26 days before slaughter.

Swine (sows)

Indication

As an aid in control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.

Dosage
3 milligrams of oxytetracycline per pound of body weight, approximately 8 hours before farrowing or immediately after completion of farrowing. Administer intramuscularly.
Limitations
Do not inject more than 5 milliliters per site. Do not use for more than 4 consecutive days. Discontinue treatment at least 26 days before slaughter.

Cattle (beef and nonlactating dairy)

Indication

Treatment of diseases due to oxytetracycline-susceptible organisms as follows: Pneumonia and shipping fever complex associated with Pasteurella species, Hemophilus species, and Klebsiella species, foot-rot and diphtheria caused by Spherophorus necrophorus, bacterial enteritis (scours) caused by Escherichia coli, wooden tongue caused by Actinobacillus lignieresi, leptospirosis caused by Leptospira pomona, and wound infections and acute metritis caused by Staphylococcus species and Streptococcus species. If labeled for use by or on the order of a licensed veterinarian, it may be used for the treatment of anaplasmosis caused by Anaplasma marginale.

Dosage
Three to 5 milligrams of oxytetracycline per pound of body weight per day; 5 milligrams per pound of body weight per day for the treatment of anaplasmosis, severe foot-rot, and severe cases of other indicated diseases. For 100-milligram-per-milliliter solution, administer intramuscularly.
Limitations
Treatment of all diseases should be instituted early and continue for 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 4 consecutive days. Consult your veterinarian if no improvement is noted within 48 hours. Do not inject more than 10 milliliters per site in adult cattle, reducing the volume according to age and body size to 0.5 to 2 milliliters in small calves. Exceeding the highest recommended dose of 5 milligrams per pound of body weight, administering at recommended levels for more than 4 consecutive days, and/or exceeding 10 milliliters intramuscularly per injection site may result in antibiotic residues beyond the withdrawal time. Discontinue treatment at least 18 days prior to slaughter. Not for use in lactating dairy cattle. This drug product is not approved for use in female dairy cattle 20 months of age or older, including dry dairy cows. Use in these cattle may cause drug residues in milk and /or in calves born to these cows.

Medamycin® 100

SPL · SPL

FDA Structured Product Label

Medamycin® 100 MEDAMYCIN®

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Cronus Pharma Specialities India Private Ltd.
NADA
108-963
Status
RX
Form
Injectable Solution
Route
Intramuscular
Species
Beef And Non-Lactating Dairy • Beef and dairy calves, excluding veal calves
Composition / specifications
Each milliliter of sterile solution contains 100 milligrams of oxytetracycline hydrochloride.

Cattle (beef, nonlactating dairy, and beef and dairy calves [excluding veal])

Indication

Treatment of bacterial pneumonia and shipping fever complex associated with Pasteurella spp.; bacterial enteritis (scours) caused by Escherichia coli; necrotic pododermatitis (foot rot) and calf diphtheria caused by Fusobacterium necrophorum; wooden tongue caused by Actinobacillus lignieresi; and wound infections, acute metritis, and traumatic injury caused by oxytetracycline-susceptible staphylococcal and streptococcal organisms.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day (3 to 5 mL per 100 pounds of body weight) by intravenous injection. Severe foot rot and the severe forms of the indicated diseases should be treated with 5 mg per pound of body weight. Treatment should be continued 24 to 48 hours following remission of disease symptoms, not to exceed a total of 4 consecutive days.

MEDAMYCIN®

SPL · SPL

FDA Structured Product Label

Medamycin® 100 MEDAMYCIN®

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Cronus Pharma Specialities India Private Ltd.
NADA
108-963
Status
RX
Form
Injectable Solution
Route
Intramuscular
Species
Beef And Non-Lactating Dairy • Beef and dairy calves, excluding veal calves
Composition / specifications
Each milliliter of sterile solution contains 100 milligrams of oxytetracycline hydrochloride.

Cattle (beef, nonlactating dairy, and beef and dairy calves [excluding veal])

Indication

Treatment of bacterial pneumonia and shipping fever complex associated with Pasteurella spp.; bacterial enteritis (scours) caused by Escherichia coli; necrotic pododermatitis (foot rot) and calf diphtheria caused by Fusobacterium necrophorum; wooden tongue caused by Actinobacillus lignieresi; and wound infections, acute metritis, and traumatic injury caused by oxytetracycline-susceptible staphylococcal and streptococcal organisms.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day (3 to 5 mL per 100 pounds of body weight) by intravenous injection. Severe foot rot and the severe forms of the indicated diseases should be treated with 5 mg per pound of body weight. Treatment should be continued 24 to 48 hours following remission of disease symptoms, not to exceed a total of 4 consecutive days.

Oxyject®

SPL · SPL

FDA Structured Product Label

Oxyject®

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Cronus Pharma Specialities India Private Ltd.
NADA
45143
Status
RX
Form
Injectable Solution
Route
Intramuscular
Species
Beef And Non-Lactating Dairy • Beef calves • Dairy calves
Composition / specifications
The drug contains 50 milligrams of oxytetracycline hydrochloride in each milliliter of sterile solution.

Cattle (beef and non-lactating dairy, beef and dairy calves)

Indication

Treatment of pneumonia and shipping fever complex associated with Pasteurella sp., Hemophilus sp., and Klebsiella sp., bacterial enteritis (scours) caused by Escherichia coli, foot rot and diphtheria caused by Spherophorus necrophorus, wooden tongue caused by Actinobacillus lignieresi, leptospirosis caused by Leptospira pomona, and wound infections, acute metritis, and traumatic injury caused by a variety of bacterial organisms (such as streptococcal and staphylococcal organisms.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day (6 to 10 mL per 100 pounds of body weight) by intramuscular injection. For leptospirosis, severe foot rot and severe forms of the indicated diseases, 5 milligrams per pound of body weight per day. Treatment should be continued 24 to 48 hours following remission of disease symptoms, not to exceed a total of 4 consecutive days.

OXYJECT® 100

SPL · SPL

FDA Structured Product Label

OXYJECT® 100 Status™ SQ

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Cronus Pharma Specialities India Private Ltd.
NADA
97452
Status
RX
Form
Injectable Solution
Route
Intramuscular
Species
No use class stated or implied • Sows with litters or about to farrow • Beef • Calves, excluding veal calves • Dairy, non-lactating
Composition / specifications
Each milliliter of sterile solution contains 100 milligrams of oxytetracycline as oxytetracycline hydrochloride.

Cattle (beef and nonlactating dairy, beef and dairy calves [excluding veal calves])

Indication

Treatment of pneumonia and shipping fever complex associated with Pasteurella spp., Haemophilus spp., and Klebsiella spp.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day (3 to 5 mL per 100 pounds of body weight) by intramuscular, subcutaneous, or intravenous injection. Treatment should be continued 24 to 48 hours following
remission of disease symptoms, not to exceed a total of 4 consecutive days.

Swine

Indication

For treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli, pneumonia caused by Pasteurella multocida, and leptospirosis caused by Leptospira pomona.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day by intramuscular or intravenous injection.

Swine (Sows)

Indication

As an aid in control of porcine colibacillosis (baby pig scours) in suckling pigs caused by Escherichia coli.

Dosage

3 milligrams of oxytetracycline per pound of body weight by intramuscular injection, approximately 8 hours before farrowing or immediately after completion of farrowing.

Status™ SQ

SPL · SPL

FDA Structured Product Label

OXYJECT® 100 Status™ SQ

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Cronus Pharma Specialities India Private Ltd.
NADA
97452
Status
RX
Form
Injectable Solution
Route
Intramuscular
Species
No use class stated or implied • Sows with litters or about to farrow • Beef • Calves, excluding veal calves • Dairy, non-lactating
Composition / specifications
Each milliliter of sterile solution contains 100 milligrams of oxytetracycline as oxytetracycline hydrochloride.

Cattle (beef and nonlactating dairy, beef and dairy calves [excluding veal calves])

Indication

Treatment of pneumonia and shipping fever complex associated with Pasteurella spp., Haemophilus spp., and Klebsiella spp.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day (3 to 5 mL per 100 pounds of body weight) by intramuscular, subcutaneous, or intravenous injection. Treatment should be continued 24 to 48 hours following
remission of disease symptoms, not to exceed a total of 4 consecutive days.

Swine

Indication

For treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli, pneumonia caused by Pasteurella multocida, and leptospirosis caused by Leptospira pomona.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day by intramuscular or intravenous injection.

Swine (Sows)

Indication

As an aid in control of porcine colibacillosis (baby pig scours) in suckling pigs caused by Escherichia coli.

Dosage

3 milligrams of oxytetracycline per pound of body weight by intramuscular injection, approximately 8 hours before farrowing or immediately after completion of farrowing.

OXY-TET 50™

SPL · SPL

FDA Structured Product Label

OXY-TET 50™ Bio-Mycin®

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Cronus Pharma Specialities India Private Ltd.
NADA
47278
Status
RX
Form
Injectable Solution
Route
Intramuscular, Intravenous
Species
No use class stated or implied • Sows • Beef And Non-Lactating Dairy
Composition / specifications
Each milliliter of sterile solution contains 50 milligrams of oxytetracycline (as oxytetracycline hydrochloride).

Cattle (beef and nonlactating dairy)

Indication

Treatment of pneumonia and shipping fever complex associated with Pasteurella sp., Hemophilus sp., and Klebsiella sp., foot rot and diphtheria caused by Spherophorus necrophorus, bacterial enteritis (scours) caused by Escherichia coli, wooden tongue caused by Actinobacillus lignieresi, leptospirosis caused by Leptospira pomona, acute metritis, anaplasmosis caused by Anaplasma marginale, and wound infections caused by Staphylococcal and Streptococcal organisms.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day (6 to 10 mL per 100 pounds of body weight) by intramuscular or intravenous injection. In severe forms of foot rot, anaplasmosis, and other severe disease forms, 5 milligrams per pound of body weight per
day (10 mL per 100 pounds of body weight). Treatment should be continued 24 to 48 hours following remission of
disease symptoms, not to exceed a total of 4 days.

Swine

Indication

For treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli, pneumonia caused by Pasteurella multocida, and leptospirosis caused by Leptospira pomona.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day (6 to 10 mL per 100 pounds of body weight) by intramuscular injection.

Swine (Sows)

Indication

As an aid in control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.

Dosage

3 milligrams of oxytetracycline per pound of body weight (6 mL per 100 lbs. body weight), by intramuscular injection, approximately 8 hours before farrowing or immediately after completion of farrowing.

Bio-Mycin®

SPL · SPL

FDA Structured Product Label

OXY-TET 50™ Bio-Mycin®

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Cronus Pharma Specialities India Private Ltd.
NADA
47278
Status
RX
Form
Injectable Solution
Route
Intramuscular, Intravenous
Species
No use class stated or implied • Sows • Beef And Non-Lactating Dairy
Composition / specifications
Each milliliter of sterile solution contains 50 milligrams of oxytetracycline (as oxytetracycline hydrochloride).

Cattle (beef and nonlactating dairy)

Indication

Treatment of pneumonia and shipping fever complex associated with Pasteurella sp., Hemophilus sp., and Klebsiella sp., foot rot and diphtheria caused by Spherophorus necrophorus, bacterial enteritis (scours) caused by Escherichia coli, wooden tongue caused by Actinobacillus lignieresi, leptospirosis caused by Leptospira pomona, acute metritis, anaplasmosis caused by Anaplasma marginale, and wound infections caused by Staphylococcal and Streptococcal organisms.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day (6 to 10 mL per 100 pounds of body weight) by intramuscular or intravenous injection. In severe forms of foot rot, anaplasmosis, and other severe disease forms, 5 milligrams per pound of body weight per
day (10 mL per 100 pounds of body weight). Treatment should be continued 24 to 48 hours following remission of
disease symptoms, not to exceed a total of 4 days.

Swine

Indication

For treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli, pneumonia caused by Pasteurella multocida, and leptospirosis caused by Leptospira pomona.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day (6 to 10 mL per 100 pounds of body weight) by intramuscular injection.

Swine (Sows)

Indication

As an aid in control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.

Dosage

3 milligrams of oxytetracycline per pound of body weight (6 mL per 100 lbs. body weight), by intramuscular injection, approximately 8 hours before farrowing or immediately after completion of farrowing.

Terramycin® 100 for Fish

SPL · SPL

FDA Structured Product Label

Terramycin® 100 for Fish Terramycin® 200 for Fish

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Phibro Animal Health Corp.
NADA
38439
Status
VFD
Form
Type A Medicated Article
Route
Oral
Species
Pacific Salmon, Reared • Freshwater-Reared Salmonids • Catfish, Reared • Freshwater-reared salmonids weighing up to 55 grams • Lobster
Composition / specifications
Type A medicated articles: 100 grams per pound. The amount of mono-alkyl (C8-C18) trimethylammonium oxytetracycline expressed is expressed in terms of an equivalent amount of oxytetracycline hydrochloride or the amount of oxytetracycline dihydrate base is expressed in terms of an equivalent amount of oxytetracycline hydrochloride.

Pacific Salmon

Indication
For marking of skeletal tissue.
Dosage

250 milligrams of Oxytetracycline per kilogram of fish per day (11.35 grams per 100 pounds of fish per day) in fish feed.

Limitations

For salmon not over 30 grams body weight. Administer as sole ration for 4 consecutive days. 

Freshwater-reared salmonids

Indication

Control of ulcer disease caused by Haemophilus piscium, furunculosis caused by Aeromonas salmonicida, bacterial hemorrhagic septicemia caused by Aeromonas hydrophila, and pseudomonas disease.

Dosage
2.5 to 3.75 grams Oxytetracycline per 100 pounds of fish per day in fish feed.
Limitations

Administer in mixed ration for 10 days. 

Catfish

Indication

Control of bacterial hemorrhagic septicemia caused by Aeromonas hydrophila and pseudomonas disease.

Dosage
2.5 to 3.75 grams Oxytetracycline per 100 pounds of fish per day in fish feed.
Limitations

Administer in mixed ration for 10 days. Do not administer when water temperature is below 16.7 degrees C (62 degrees F).

Freshwater-reared salmonids

Indication
Control of mortality due to coldwater disease associated with Flavobacterium psychrophilum.
Dosage

3.75 g oxytetracycline per 100 lb of fish per day for 10 days.

Limitations

Administer in mixed ration for 10 days. 

Freshwater-reared salmonids

Indication

Control of mortality due to columnaris disease associated with Flavobacterium columnare.

Dosage

3.75 g oxytetracycline per 100 lb of fish per day for 10 days.

Limitations

Administer in mixed ration for 10 days. 

Lobster

Indication
Control of gaffkemia caused by Aerococcus viridans.
Dosage
1 gram Oxytetracycline per pound of medicated feed in fish feed.
Limitations
Administer as sole ration for 5 consecutive days.

Freshwater-reared salmonids weighing up to 55 grams

Indication

For marking the skeletal tissue

Dosage

3.75 g oxytetracycline per 100 lb of fish per day for 10 days. Feed for 10 days.

Catfish

Indication

Control of mortality due to columnaris disease associated with Flavobacterium columnare

Dosage

3.75 g oxytetracycline per 100 lb of fish per day for 10 days. Administer in mixed ration for 10 days. Do not administer when water temperature is below 16.7 degrees C (62 degrees F).

Terramycin® 200 for Fish

SPL · SPL

FDA Structured Product Label

Terramycin® 100 for Fish Terramycin® 200 for Fish

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Phibro Animal Health Corp.
NADA
38439
Status
VFD
Form
Type A Medicated Article
Route
Oral
Species
Pacific Salmon, Reared • Freshwater-Reared Salmonids • Catfish, Reared • Freshwater-reared salmonids weighing up to 55 grams • Lobster
Composition / specifications
Type A medicated articles: 100 grams per pound. The amount of mono-alkyl (C8-C18) trimethylammonium oxytetracycline expressed is expressed in terms of an equivalent amount of oxytetracycline hydrochloride or the amount of oxytetracycline dihydrate base is expressed in terms of an equivalent amount of oxytetracycline hydrochloride.

Pacific Salmon

Indication
For marking of skeletal tissue.
Dosage

250 milligrams of Oxytetracycline per kilogram of fish per day (11.35 grams per 100 pounds of fish per day) in fish feed.

Limitations

For salmon not over 30 grams body weight. Administer as sole ration for 4 consecutive days. 

Freshwater-reared salmonids

Indication

Control of ulcer disease caused by Haemophilus piscium, furunculosis caused by Aeromonas salmonicida, bacterial hemorrhagic septicemia caused by Aeromonas hydrophila, and pseudomonas disease.

Dosage
2.5 to 3.75 grams Oxytetracycline per 100 pounds of fish per day in fish feed.
Limitations

Administer in mixed ration for 10 days. 

Catfish

Indication

Control of bacterial hemorrhagic septicemia caused by Aeromonas hydrophila and pseudomonas disease.

Dosage
2.5 to 3.75 grams Oxytetracycline per 100 pounds of fish per day in fish feed.
Limitations

Administer in mixed ration for 10 days. Do not administer when water temperature is below 16.7 degrees C (62 degrees F).

Freshwater-reared salmonids

Indication
Control of mortality due to coldwater disease associated with Flavobacterium psychrophilum.
Dosage

3.75 g oxytetracycline per 100 lb of fish per day for 10 days.

Limitations

Administer in mixed ration for 10 days. 

Freshwater-reared salmonids

Indication

Control of mortality due to columnaris disease associated with Flavobacterium columnare.

Dosage

3.75 g oxytetracycline per 100 lb of fish per day for 10 days.

Limitations

Administer in mixed ration for 10 days. 

Lobster

Indication
Control of gaffkemia caused by Aerococcus viridans.
Dosage
1 gram Oxytetracycline per pound of medicated feed in fish feed.
Limitations
Administer as sole ration for 5 consecutive days.

Freshwater-reared salmonids weighing up to 55 grams

Indication

For marking the skeletal tissue

Dosage

3.75 g oxytetracycline per 100 lb of fish per day for 10 days. Feed for 10 days.

Catfish

Indication

Control of mortality due to columnaris disease associated with Flavobacterium columnare

Dosage

3.75 g oxytetracycline per 100 lb of fish per day for 10 days. Administer in mixed ration for 10 days. Do not administer when water temperature is below 16.7 degrees C (62 degrees F).

Tetroxy® HCA-280

SPL · SPL

FDA Structured Product Label

Tetroxy® HCA-280 Tetroxy® HCA-1772 Tetroxy® HCA-1400

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Bimeda Animal Health Limited
ANADA
200-144
Status
RX
Form
Soluble Powder
Route
Oral
Species
Breeding • No use class stated or implied • Growing • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption
Composition / specifications
Each 2.73 grams of powder contains 1 gram of oxytetracycline hydrochloride (packets: 9.87 oz, 3.09 lb and 3.91 lb)

Chickens

Indication

Control of chronic respiratory disease (CRD) and air sac infections caused by Mycoplasma gallisepticum and E. coli susceptible to oxytetracycline; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

400 to 800 milligrams per gallon of drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Indication

Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage

200 to 400 milligrams per gallon of drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Turkeys

Indication

Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage

400 milligrams per gallon of drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Indication

Control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.

Dosage

200 to 400 milligrams per gallon of drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Turkeys (growing)

Indication

Control of complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis) susceptible to oxytetracycline.

Dosage

25 milligrams per pound of body weight in drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Swine

Indication

Control and treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily in drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Use as sole source of OTC. Administer up to 5 days. Do not use for more than 5 consecutive days.

Swine (breeding stock)

Indication

Control and treatment of leptospirosis (reducing the incidence of abortions and shedding of leptospira) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily in drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Use as sole source of OTC. Administer up to 5 days. Do not use for more than 5 consecutive days.

Tetroxy® HCA-1772

SPL · SPL

FDA Structured Product Label

Tetroxy® HCA-280 Tetroxy® HCA-1772 Tetroxy® HCA-1400

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Bimeda Animal Health Limited
ANADA
200-144
Status
RX
Form
Soluble Powder
Route
Oral
Species
Breeding • No use class stated or implied • Growing • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption
Composition / specifications
Each 2.73 grams of powder contains 1 gram of oxytetracycline hydrochloride (packets: 9.87 oz, 3.09 lb and 3.91 lb)

Chickens

Indication

Control of chronic respiratory disease (CRD) and air sac infections caused by Mycoplasma gallisepticum and E. coli susceptible to oxytetracycline; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

400 to 800 milligrams per gallon of drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Indication

Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage

200 to 400 milligrams per gallon of drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Turkeys

Indication

Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage

400 milligrams per gallon of drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Indication

Control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.

Dosage

200 to 400 milligrams per gallon of drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Turkeys (growing)

Indication

Control of complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis) susceptible to oxytetracycline.

Dosage

25 milligrams per pound of body weight in drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Swine

Indication

Control and treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily in drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Use as sole source of OTC. Administer up to 5 days. Do not use for more than 5 consecutive days.

Swine (breeding stock)

Indication

Control and treatment of leptospirosis (reducing the incidence of abortions and shedding of leptospira) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily in drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Use as sole source of OTC. Administer up to 5 days. Do not use for more than 5 consecutive days.

Tetroxy® HCA-1400

SPL · SPL

FDA Structured Product Label

Tetroxy® HCA-280 Tetroxy® HCA-1772 Tetroxy® HCA-1400

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Bimeda Animal Health Limited
ANADA
200-144
Status
RX
Form
Soluble Powder
Route
Oral
Species
Breeding • No use class stated or implied • Growing • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption
Composition / specifications
Each 2.73 grams of powder contains 1 gram of oxytetracycline hydrochloride (packets: 9.87 oz, 3.09 lb and 3.91 lb)

Chickens

Indication

Control of chronic respiratory disease (CRD) and air sac infections caused by Mycoplasma gallisepticum and E. coli susceptible to oxytetracycline; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

400 to 800 milligrams per gallon of drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Indication

Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage

200 to 400 milligrams per gallon of drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Turkeys

Indication

Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage

400 milligrams per gallon of drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Indication

Control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.

Dosage

200 to 400 milligrams per gallon of drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Turkeys (growing)

Indication

Control of complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis) susceptible to oxytetracycline.

Dosage

25 milligrams per pound of body weight in drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Swine

Indication

Control and treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily in drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Use as sole source of OTC. Administer up to 5 days. Do not use for more than 5 consecutive days.

Swine (breeding stock)

Indication

Control and treatment of leptospirosis (reducing the incidence of abortions and shedding of leptospira) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily in drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Use as sole source of OTC. Administer up to 5 days. Do not use for more than 5 consecutive days.

Noromycin® 300 LA

SPL · SPL

FDA Structured Product Label

Noromycin® 300 LA

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Norbrook Laboratories, Ltd.
NADA
141-143
Status
RX
Form
Solution
Route
Intravenous, Subcutaneous, Intramuscular
Species
No use class stated or implied • Sows • Calves, Including Prerumenative Veal • Beef • Dairy, non-lactating
Composition / specifications
Each mL of solution contains 300 mg oxytetracycline base.

Beef Cattle, Non-lactating Dairy Cattle, and Calves including Pre-ruminating (Veal) Calves

Indication

For treatment of bacterial pneumonia caused by Pasteurella species (shipping fever) in calves and yearlings where treatment is impractical due to husbandry conditions, such as cattle on range, or where their repeated restraint is inadvisable; or for treatment of infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis.

Dosage

9 to 13.6 milligrams per pound of body weight. Administer once intramuscularly or subcutaneously.

Indication

For control of respiratory disease in cattle at high risk of developing bovine respiratory disease associated with Mannheimia (Pasteurella) haemolytica.

Dosage

13.6 milligrams per pound of body weight. Administer once intramuscularly or subcutaneously.

Indication

For treatment of pneumonia and shipping fever complex associated with Pasteurella species and Histophilus species, foot-rot and diphtheria caused by Fusobacterium necrophorum, bacterial enteritis (scours) caused by Escherichia coli, wooden tongue caused by Actinobacillus lignieresii, leptospirosis caused by Leptospira pomona, and wound infections and acute metritis caused by strains of staphylococcal and streptococcal organisms sensitive to oxytetracycline.

Dosage

3 to 5 milligrams per pound of body weight per day. For treatment of severe foot-rot and advanced cases of other indicated diseases, 5 milligrams per pound of body weight per day. Administer intramuscularly, subcutaneously, or intravenously. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days.

Swine

Indication

For treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli, pneumonia caused by Pasteurella multocida, and leptospirosis caused by Leptospira pomona.

Dosage

3 to 5 milligrams per pound of body weight per day. Administer intramuscularly. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days.

Indication

For treatment of pneumonia caused by Pasteurella multocida where retreatment for pneumonia is impractical.

Dosage

9 milligrams per pound of body weight. Administer once intramuscularly.

Swine (Sows)

Indication

As an aid in control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.

Dosage

3 milligrams per pound of body weight. Administer once intramuscularly approximately 8 hours before farrowing or immediately after completion of farrowing.

Biocyl-50

SPL · SPL

FDA Structured Product Label

Biocyl-50 Biocyl-100

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Bimeda Animal Health Limited
NADA
140-582
Status
RX
Form
Injectable Solution
Route
Intravenous
Species
Beef • Dairy, non-lactating
Composition / specifications
Each mL contains 50 mg of oxytetracycline hydrochloride

Cattle (Beef and Non-Lactating Dairy)

Indication
Treatment of diseases due to oxytetracycline-susceptible organisms as follows: pneumonia and shipping fever complex associated with Pasteurella species and Hemophilus species; foot rot and diphtheria caused by Fusobacterium necrophorum; bacterial enteritis (scours) caused by Escherichia coli; wooden tongue caused by Actinobacillus lignieresii; leptospirosis caused by Leptospira Pomona; acute metritis and wound infections caused by staphylococcal and streptococcal organisms; if labeled for use by or on the order of a licensed veterinarian, it may be used for treatment of anaplasmosis caused by Anaplasma marginale and anthrax caused by Bacillus anthracis.
Dosage
3 to 5 milligrams per pound of body weight daily, 5 milligrams per pound for anaplasmosis, severe foot rot, and severe forms of other diseases. Administer by intravenous injection.
Limitations

Treatment should be continued 24 to 48 hours following remission of disease symptoms, but not to exceed a total of 4 consecutive days. If no improvement occurs within 24 to 48 hours, reevaluate diagnosis and therapy. Discontinue use at least 19 days prior to slaughter. This drug product is not approved for use in female dairy cattle 20months of age or older, including dry dairy cows. Use in these cattle may cause drug residues in milk and/or in calves born to these cows.

Biocyl-100

SPL · SPL

FDA Structured Product Label

Biocyl-50 Biocyl-100

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Bimeda Animal Health Limited
NADA
140-582
Status
RX
Form
Injectable Solution
Route
Intravenous
Species
Beef • Dairy, non-lactating
Composition / specifications
Each mL contains 50 mg of oxytetracycline hydrochloride

Cattle (Beef and Non-Lactating Dairy)

Indication
Treatment of diseases due to oxytetracycline-susceptible organisms as follows: pneumonia and shipping fever complex associated with Pasteurella species and Hemophilus species; foot rot and diphtheria caused by Fusobacterium necrophorum; bacterial enteritis (scours) caused by Escherichia coli; wooden tongue caused by Actinobacillus lignieresii; leptospirosis caused by Leptospira Pomona; acute metritis and wound infections caused by staphylococcal and streptococcal organisms; if labeled for use by or on the order of a licensed veterinarian, it may be used for treatment of anaplasmosis caused by Anaplasma marginale and anthrax caused by Bacillus anthracis.
Dosage
3 to 5 milligrams per pound of body weight daily, 5 milligrams per pound for anaplasmosis, severe foot rot, and severe forms of other diseases. Administer by intravenous injection.
Limitations

Treatment should be continued 24 to 48 hours following remission of disease symptoms, but not to exceed a total of 4 consecutive days. If no improvement occurs within 24 to 48 hours, reevaluate diagnosis and therapy. Discontinue use at least 19 days prior to slaughter. This drug product is not approved for use in female dairy cattle 20months of age or older, including dry dairy cows. Use in these cattle may cause drug residues in milk and/or in calves born to these cows.

Oxytetracycline-50

SPL · SPL

FDA Structured Product Label

Oxytetracycline-50

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Huvepharma EOOD
NADA
48287
Status
RX
Form
Liquid (Solution)
Route
Intramuscular
Species
Beef • Calves • Dairy, non-lactating
Composition / specifications
Each milliliter of sterile solution contains 50 milligrams of oxytetracycline hydrochloride.

Cattle (beef, beef calves, nonlactating dairy, dairy calves)

Indication
The drug is used for treatment of bacterial pneumonia and shipping fever complex associated with Pasteurella species; foot-rot and diphtheria caused by Spherophorus necrophorus; bacterial enteritis (scours) caused by Escherichia coli; wooden tongue caused by Actinobacillus lignieresi; wound infections and acute metritis caused by staphylococcal and streptococcal organisms susceptible to oxytetracycline.
Dosage
Administer 3 to 5 milligrams of the oxytetracycline hydrochloride intramuscularly per pound of body weight per day. In severe forms of the indicated diseases, administer the equivalent of 5 milligrams of oxytetracycline hydrochloride per pound of body weight per day. Continue treatment 24 to 48 hours following remission of disease symptoms, not to exceed a total of 4 consecutive days. Reduce the volume administered per injection site according to age and body size. In calves weighing 100 pounds or less inject only 2 milliliters per site.
Limitations

If no improvement is noted within 24 to 48 hours, consult a veterinarian for diagnosis and therapy. In adult livestock, do not inject more than 10 milliliters at any one site. Rapid intravenous administration may result in animal collapse. Oxytetracycline should be administered intravenously slowly over a period of at least5 minutes.

Rachelle Oxyvet Injection

SPL · SPL

FDA Structured Product Label

Rachelle Oxyvet Injection

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Zoetis Inc.
NADA
91127
Status
RX
Form
Liquid (Solution)
Route
Intravenous, Intramuscular
Species
Beef • Calves • Dairy, non-lactating
Composition / specifications
Each milliliter of sterile solution contains 100 milligrams of oxytetracycline hydrochloride.

Cattle (beef and nonlactating dairy)

Indication
Treatment of diseases due to oxytetracycline-susceptible organisms as follows: Pneumonia and shipping fever complex associated with Pasteurella species and Hemophilus species, foot-rot and diphtheria caused by Fusobacterium necrophorum, bacterial enteritis (scours) caused by Escherichia coli, wooden tongue caused by Actinobacillus lignieresii, leptospirosis caused by Leptospira pomona, and wound infections and acute metritis caused by Staphylococcus species and Streptococcus species. If labeled for use by or on the order of a licensed veterinarian, it may be used for the treatment of anaplasmosis caused by Anaplasma marginale and anthrax caused by Bacillus anthracis.
Dosage
3 to 5 milligrams of oxytetracycline per pound of body weight per day; 5 milligrams per pound of body weight per day for treatment of anaplasmosis, severe foot-rot, and severe cases of other indicated diseases. Administer intramuscularly.
Limitations
Treatment of all diseases should be instituted early and continue for 24 to 48 hours beyond remission of disease symptoms but not to exceed a total of 4 consecutive days. Consult your veterinarian if no improvement is noted within 48 hours. Do not inject more than 10 milliliters per site in adult cattle, reducing the volume according to age and body size to 1 to 2 milliliters in small calves. Exceeding the highest recommended dose of 5 milligrams per pound of body weight, administering at recommended levels for more than 4 consecutive days, and/or exceeding 10 milliliters intramuscularly per injection site may result in antibiotic residues beyond the withdrawal time. Discontinue treatment at least 15 days prior to slaughter. Not for use in lactating dairy cattle.

Oxyvet-100

SPL · SPL

FDA Structured Product Label

Oxyvet-100 Aquachel-100

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Zoetis Inc.
NADA
99402
Status
RX
Form
Liquid (Solution)
Route
Intravenous
Species
Beef • Calves • Dairy, non-lactating
Composition / specifications
The drug contains 100 milligrams of oxytetracycline hydrochloride in each milliliter of sterile solution.

Cattle (beef and nonlactating dairy)

Indication
The drug is intended for use in the treatment of disease due to oxytetracycline-susceptible organisms in beef cattle and non-lactating dairy cattle. It is indicated in the treatment of pneumonia and shipping fever complex associated with Pasteurella species, Hemophilus species, Klebsiella species, foot-rot and diphtheria caused by Spherophorus necrophorus, bacterial enteritis (scours) caused by Escherichia coli, wooden tongue caused by Actinobacillus lignieresi, acute metritis, and wound infections caused by staphylococcal and streptococcal organisms.
Dosage
It is administered to cattle at a dosage level of 3 to 5 milligrams per pound of body weight per day. It is administered intravenously from a 100 milligram per milliliter solution. Severe foot-rot and the severe forms of the indicated diseases should be treated with 5 milligrams per pound of body weight. Treatment should be continued 24 to 48 hours following remission of disease symptoms, however, not to exceed a total of 4 consecutive days. If no improvement is noted within 24 hours consult a veterinarian. When injecting the drug intramuscularly do not inject more than 10 milliliters per site in adult cattle. Reduce the amount injected at each site according to the size of the animal. For very small calves do not use more than 2 milliliters per injection site.
Limitations
Not for use in lactating dairy cattle. Discontinue treatment at least 19 days prior to slaughter. When administered intramuscularly within 30 days of slaughter, muscle discoloration may necessitate trimming of the injection site and surrounding tissues.

Aquachel-100

SPL · SPL

FDA Structured Product Label

Oxyvet-100 Aquachel-100

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Zoetis Inc.
NADA
99402
Status
RX
Form
Liquid (Solution)
Route
Intravenous
Species
Beef • Calves • Dairy, non-lactating
Composition / specifications
The drug contains 100 milligrams of oxytetracycline hydrochloride in each milliliter of sterile solution.

Cattle (beef and nonlactating dairy)

Indication
The drug is intended for use in the treatment of disease due to oxytetracycline-susceptible organisms in beef cattle and non-lactating dairy cattle. It is indicated in the treatment of pneumonia and shipping fever complex associated with Pasteurella species, Hemophilus species, Klebsiella species, foot-rot and diphtheria caused by Spherophorus necrophorus, bacterial enteritis (scours) caused by Escherichia coli, wooden tongue caused by Actinobacillus lignieresi, acute metritis, and wound infections caused by staphylococcal and streptococcal organisms.
Dosage
It is administered to cattle at a dosage level of 3 to 5 milligrams per pound of body weight per day. It is administered intravenously from a 100 milligram per milliliter solution. Severe foot-rot and the severe forms of the indicated diseases should be treated with 5 milligrams per pound of body weight. Treatment should be continued 24 to 48 hours following remission of disease symptoms, however, not to exceed a total of 4 consecutive days. If no improvement is noted within 24 hours consult a veterinarian. When injecting the drug intramuscularly do not inject more than 10 milliliters per site in adult cattle. Reduce the amount injected at each site according to the size of the animal. For very small calves do not use more than 2 milliliters per injection site.
Limitations
Not for use in lactating dairy cattle. Discontinue treatment at least 19 days prior to slaughter. When administered intramuscularly within 30 days of slaughter, muscle discoloration may necessitate trimming of the injection site and surrounding tissues.

Terramycin® 100

SPL · SPL

FDA Structured Product Label

Terramycin® 100 Liquamycin® 100

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Zoetis Inc.
NADA
94114
Status
RX
Form
Liquid (Solution)
Route
Intramuscular
Species
No use class stated or implied • Sows with litters or about to farrow • Beef • Calves • Dairy, non-lactating
Composition / specifications
Each milliliter of sterile solution contains 100 milligrams of oxytetracycline hydrochloride.

Swine

Indication
For treatment of bacterial enteritis (scours colibacillosis) caused by Escherichia coli, pneumonia caused by Pasteurella multocida, and leptospirosis caused by Leptospira pomona.
Dosage
3 to 5 milligrams of oxytetracycline per pound of body weight per day. Administer intramuscularly.
Limitations
Do not inject more than 5 milliliters per site in adult swine, reducing the volume according to age and body size to 1 to 2 milliliters in young pigs. Discontinue treatment at least 22 days prior to slaughter.

Swine (sows with litters or about to farrow)

Indication
As an aid in control of infections enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.
Dosage
3 milligrams of oxytetracycline per pound of body weight, administered once, approximately 8 hours before farrowing or immediately after completion of farrowing. Administer intramuscularly.
Limitations
Do not inject more than 5 milliliters per site in adult swine, reducing the volume according to age and body size to 1 to 2 milliliters in young pigs. Discontinue treatment at least 22 days prior to slaughter.

Cattle (beef and nonlactating dairy)

Indication
Treatment of diseases due to oxytetracycline-susceptible organisms as follows: Pneumonia and shipping fever complex associated with Pasteurella species and Hemophilus species, foot-rot and diphtheria caused by Fusobacterium necrophorum, bacterial enteritis (scours) caused by Escherichia coli, wooden tongue caused by Actinobacillus lignieresii, leptospirosis caused by Leptospira pomona, and wound infections and acute metritis caused by Staphylococcus species and Streptococcus species If labeled for use by or on the order of a licensed veterinarian, it may be used for the treatment of anaplasmosis caused by Anaplasma marginale and anthrax caused by Bacillus anthracis.
Dosage
3 to 5 milligrams of oxytetracycline per pound of body weight per day; 5 milligrams per pound of body weight per day for treatment of anaplasmosis, severe foot-rot, and severe cases of other indicated diseases. Administer intramuscularly.
Limitations
Treatment of all diseases should be instituted early and continue for 24 to 48 hours beyond remission of disease symptoms but not to exceed a total of 4 consecutive days. Consult your veterinarian if no improvement is noted within 48 hours. Do not inject more than 10 milliliters per site in adult cattle, reducing the volume according to age and body size to 1 to 2 milliliters in small calves. Exceeding the highest recommended dose of 5 milligrams per pound of body weight, administering at recommended levels for more than 4 consecutive days, and/or exceeding 10 milliliters intramuscularly per injection site may result in antibiotic residues beyond the withdrawal time. Discontinue treatment at least 15 days prior to slaughter. Not for use in lactating dairy cattle.

Liquamycin® 100

SPL · SPL

FDA Structured Product Label

Terramycin® 100 Liquamycin® 100

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Zoetis Inc.
NADA
94114
Status
RX
Form
Liquid (Solution)
Route
Intramuscular
Species
No use class stated or implied • Sows with litters or about to farrow • Beef • Calves • Dairy, non-lactating
Composition / specifications
Each milliliter of sterile solution contains 100 milligrams of oxytetracycline hydrochloride.

Swine

Indication
For treatment of bacterial enteritis (scours colibacillosis) caused by Escherichia coli, pneumonia caused by Pasteurella multocida, and leptospirosis caused by Leptospira pomona.
Dosage
3 to 5 milligrams of oxytetracycline per pound of body weight per day. Administer intramuscularly.
Limitations
Do not inject more than 5 milliliters per site in adult swine, reducing the volume according to age and body size to 1 to 2 milliliters in young pigs. Discontinue treatment at least 22 days prior to slaughter.

Swine (sows with litters or about to farrow)

Indication
As an aid in control of infections enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.
Dosage
3 milligrams of oxytetracycline per pound of body weight, administered once, approximately 8 hours before farrowing or immediately after completion of farrowing. Administer intramuscularly.
Limitations
Do not inject more than 5 milliliters per site in adult swine, reducing the volume according to age and body size to 1 to 2 milliliters in young pigs. Discontinue treatment at least 22 days prior to slaughter.

Cattle (beef and nonlactating dairy)

Indication
Treatment of diseases due to oxytetracycline-susceptible organisms as follows: Pneumonia and shipping fever complex associated with Pasteurella species and Hemophilus species, foot-rot and diphtheria caused by Fusobacterium necrophorum, bacterial enteritis (scours) caused by Escherichia coli, wooden tongue caused by Actinobacillus lignieresii, leptospirosis caused by Leptospira pomona, and wound infections and acute metritis caused by Staphylococcus species and Streptococcus species If labeled for use by or on the order of a licensed veterinarian, it may be used for the treatment of anaplasmosis caused by Anaplasma marginale and anthrax caused by Bacillus anthracis.
Dosage
3 to 5 milligrams of oxytetracycline per pound of body weight per day; 5 milligrams per pound of body weight per day for treatment of anaplasmosis, severe foot-rot, and severe cases of other indicated diseases. Administer intramuscularly.
Limitations
Treatment of all diseases should be instituted early and continue for 24 to 48 hours beyond remission of disease symptoms but not to exceed a total of 4 consecutive days. Consult your veterinarian if no improvement is noted within 48 hours. Do not inject more than 10 milliliters per site in adult cattle, reducing the volume according to age and body size to 1 to 2 milliliters in small calves. Exceeding the highest recommended dose of 5 milligrams per pound of body weight, administering at recommended levels for more than 4 consecutive days, and/or exceeding 10 milliliters intramuscularly per injection site may result in antibiotic residues beyond the withdrawal time. Discontinue treatment at least 15 days prior to slaughter. Not for use in lactating dairy cattle.

Terramycin® Scours Tablets

SPL · SPL

FDA Structured Product Label

Terramycin® Scours Tablets

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Zoetis Inc.
NADA
11060
Status
RX
Form
Tablet
Route
Oral
Species
Beef calves • Dairy calves
Composition / specifications
Each tablet contains 250 of oxytetracycline hydrochloride

Cattle (beef and dairy calves)

Indication

For treatment of bacterial enteritis caused by Salmonella typhimurium and Escherichia coli (colibacillosis) and bacterial pneumonia (shipping fever complex, pasteurellosis) caused by Pasteurella multocida.

Dosage

Orally administer 2 tablets per 100 lb of body weight every 12 hours (10 mg/lb of body weight daily in divided doses) for up to 4 consecutive days. Dosage should continue until the animal returns to normal and for 24-48 hours after symptoms have subsided. Treatment should not exceed 4 consecutive days.

Indication

For control of bacterial enteritis caused by Salmonella typhimurium and Escherichia coli (colibacillosis) and bacterial pneumonia (shipping fever complex, pasteurellosis) caused by Pasteurella multocida.

Dosage

Orally administer 1 tablet per 100 lb of body weight every 12 hours (5 mg/lb of body weight daily in divided doses) for up to 4 consecutive days. Dosage should continue until the animal returns to normal and for 24-48 hours after symptoms have subsided. Treatment should not exceed 4 consecutive days.

TM-50®

SPL · SPL

FDA Structured Product Label

TM-50® TM-50® D TM-100® TM-100®D

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Phibro Animal Health Corp.
NADA
8804
Status
VFD
Form
Type A Medicated Article
Route
Oral
Species
Honey Bees • Breeding • No use class stated or implied • Beef • Calves • Dairy, non-lactating • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Lobster • Sheep, No Use Class Stated Or Implied
Composition / specifications
Type A medicated articles containing 50 grams oxytetracycline (from oxytetracycline quaternary salt) equivalent to oxytetracycline hydrochloride per pound

Chickens

Indication
For reduction of mortality due to air sacculitis (air-sac infection) caused by E. coli susceptible to oxytetracycline.
Dosage
500 grams per ton of feed.
Limitations

Feed continuously for 5 days. Do not administer to chickens producing eggs for human consumption. Withdraw 24 hours before slaughter. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues.

Indication
For control of chronic respiratory disease (CRD) and air sac infection caused by M. gallisepticum and Escherichia coli susceptible to oxytetracycline.
Dosage
400 grams per ton of feed.
Limitations

Feed continuously for 7 to 14 days. Do not administer to chickens producing eggs for human consumption. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues.

Indication
Control of infectious synovitis caused by Mycoplasma synoviae; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.
Dosage
100 - 200 grams per ton of feed.
Limitations

Feed continuously for 7 to 14 days. Do not administer to chickens producing eggs for human consumption. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues.

Turkeys

Indication
For control of complicating bacterial organisms associated with bluecomb (transmissible enteritis; coronaviral enteritis) susceptible to oxytetracycline.
Dosage
25 milligrams per pound of body weight.
Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not administer to turkeys producing eggs for human consumption.

Indication
For control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.
Dosage
100 grams per ton of feed.
Limitations

Feed continuously for 7 to 14 days. Do not administer to turkeys producing eggs for human consumption.

Indication
For control of infectious synovitis caused by M. synoviae susceptible to oxytetracycline.
Dosage
200 grams per ton of feed.
Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not administer to turkeys producing eggs for human consumption.

Swine

Indication
For treatment of bacterial enteritis caused by E. coli and Salmonella choleraesuis susceptible to oxytetracycline and treatment of bacterial pneumonia caused by P. multocida susceptible to oxytetracycline.
Dosage
10 milligrams per pound of body weight.
Limitations

Feed continuously for 7 to 14 days. 

Swine (Breeding)

Indication

For control and treatment of leptospirosis (reducing the incidence of abortion and shedding of leptospirae) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight.
Limitations

Feed continuously for not more than 14 days.  

Cattle (beef and non-lactating dairy: growing cattle over 400 pounds)

Indication

For the reduction of the incidence of liver abscesses.

Dosage

75 milligrams per head per day.

Limitations

Feed continuously.

Cattle (calves including veal calves, beef, and non-lactating dairy)

Indication

Treatment of bacterial enteritis caused by E. coli.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. In milk replacer or starter feed. Withdraw 0 days before slaughter. When used in milk replacers, the treatment claim (10 mg/lb) is limited to bacterial enteritis caused by E. coli only.

Indication

Treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline).

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Withdraw 0 days before slaughter.

Indication
For prevention and treatment of the early stages of shipping fever complex.
Dosage
0.5 - 2.0 grams per head per day in feed.
Limitations

Feed 3 to 5 days before and after arrival in feedlots. 

Sheep

Indication

For treatment of bacterial enteritis caused by E. coli and bacterial pneumonia caused by P. multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter.

Lobsters

Indication
For control of gaffkemia caused by Aerococcus viridans.
Dosage
1 gram per pound medicated feed.
Limitations

Administer as sole ration for 5 consecutive days. Withdraw medicated feed 30 days before harvesting lobsters.

Honey bees

Indication

Control of American Foulbrood caused by Bacillus larvae, and European foulbrood caused by Streptococcus pluton susceptible to oxytetracycline.

Dosage

200 milligrams per colony.

Limitations

Remove at least 6 weeks prior to main honey flow.

TM-50® D

SPL · SPL

FDA Structured Product Label

TM-50® TM-50® D TM-100® TM-100®D

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Phibro Animal Health Corp.
NADA
8804
Status
VFD
Form
Type A Medicated Article
Route
Oral
Species
Honey Bees • Breeding • No use class stated or implied • Beef • Calves • Dairy, non-lactating • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Lobster • Sheep, No Use Class Stated Or Implied
Composition / specifications
Type A medicated articles containing 50 grams oxytetracycline (from oxytetracycline quaternary salt) equivalent to oxytetracycline hydrochloride per pound

Chickens

Indication
For reduction of mortality due to air sacculitis (air-sac infection) caused by E. coli susceptible to oxytetracycline.
Dosage
500 grams per ton of feed.
Limitations

Feed continuously for 5 days. Do not administer to chickens producing eggs for human consumption. Withdraw 24 hours before slaughter. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues.

Indication
For control of chronic respiratory disease (CRD) and air sac infection caused by M. gallisepticum and Escherichia coli susceptible to oxytetracycline.
Dosage
400 grams per ton of feed.
Limitations

Feed continuously for 7 to 14 days. Do not administer to chickens producing eggs for human consumption. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues.

Indication
Control of infectious synovitis caused by Mycoplasma synoviae; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.
Dosage
100 - 200 grams per ton of feed.
Limitations

Feed continuously for 7 to 14 days. Do not administer to chickens producing eggs for human consumption. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues.

Turkeys

Indication
For control of complicating bacterial organisms associated with bluecomb (transmissible enteritis; coronaviral enteritis) susceptible to oxytetracycline.
Dosage
25 milligrams per pound of body weight.
Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not administer to turkeys producing eggs for human consumption.

Indication
For control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.
Dosage
100 grams per ton of feed.
Limitations

Feed continuously for 7 to 14 days. Do not administer to turkeys producing eggs for human consumption.

Indication
For control of infectious synovitis caused by M. synoviae susceptible to oxytetracycline.
Dosage
200 grams per ton of feed.
Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not administer to turkeys producing eggs for human consumption.

Swine

Indication
For treatment of bacterial enteritis caused by E. coli and Salmonella choleraesuis susceptible to oxytetracycline and treatment of bacterial pneumonia caused by P. multocida susceptible to oxytetracycline.
Dosage
10 milligrams per pound of body weight.
Limitations

Feed continuously for 7 to 14 days. 

Swine (Breeding)

Indication

For control and treatment of leptospirosis (reducing the incidence of abortion and shedding of leptospirae) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight.
Limitations

Feed continuously for not more than 14 days.  

Cattle (beef and non-lactating dairy: growing cattle over 400 pounds)

Indication

For the reduction of the incidence of liver abscesses.

Dosage

75 milligrams per head per day.

Limitations

Feed continuously.

Cattle (calves including veal calves, beef, and non-lactating dairy)

Indication

Treatment of bacterial enteritis caused by E. coli.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. In milk replacer or starter feed. Withdraw 0 days before slaughter. When used in milk replacers, the treatment claim (10 mg/lb) is limited to bacterial enteritis caused by E. coli only.

Indication

Treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline).

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Withdraw 0 days before slaughter.

Indication
For prevention and treatment of the early stages of shipping fever complex.
Dosage
0.5 - 2.0 grams per head per day in feed.
Limitations

Feed 3 to 5 days before and after arrival in feedlots. 

Sheep

Indication

For treatment of bacterial enteritis caused by E. coli and bacterial pneumonia caused by P. multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter.

Lobsters

Indication
For control of gaffkemia caused by Aerococcus viridans.
Dosage
1 gram per pound medicated feed.
Limitations

Administer as sole ration for 5 consecutive days. Withdraw medicated feed 30 days before harvesting lobsters.

Honey bees

Indication

Control of American Foulbrood caused by Bacillus larvae, and European foulbrood caused by Streptococcus pluton susceptible to oxytetracycline.

Dosage

200 milligrams per colony.

Limitations

Remove at least 6 weeks prior to main honey flow.

TM-100®

SPL · SPL

FDA Structured Product Label

TM-50® TM-50® D TM-100® TM-100®D

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Phibro Animal Health Corp.
NADA
8804
Status
VFD
Form
Type A Medicated Article
Route
Oral
Species
Honey Bees • Breeding • No use class stated or implied • Beef • Calves • Dairy, non-lactating • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Lobster • Sheep, No Use Class Stated Or Implied
Composition / specifications
Type A medicated articles containing 50 grams oxytetracycline (from oxytetracycline quaternary salt) equivalent to oxytetracycline hydrochloride per pound

Chickens

Indication
For reduction of mortality due to air sacculitis (air-sac infection) caused by E. coli susceptible to oxytetracycline.
Dosage
500 grams per ton of feed.
Limitations

Feed continuously for 5 days. Do not administer to chickens producing eggs for human consumption. Withdraw 24 hours before slaughter. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues.

Indication
For control of chronic respiratory disease (CRD) and air sac infection caused by M. gallisepticum and Escherichia coli susceptible to oxytetracycline.
Dosage
400 grams per ton of feed.
Limitations

Feed continuously for 7 to 14 days. Do not administer to chickens producing eggs for human consumption. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues.

Indication
Control of infectious synovitis caused by Mycoplasma synoviae; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.
Dosage
100 - 200 grams per ton of feed.
Limitations

Feed continuously for 7 to 14 days. Do not administer to chickens producing eggs for human consumption. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues.

Turkeys

Indication
For control of complicating bacterial organisms associated with bluecomb (transmissible enteritis; coronaviral enteritis) susceptible to oxytetracycline.
Dosage
25 milligrams per pound of body weight.
Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not administer to turkeys producing eggs for human consumption.

Indication
For control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.
Dosage
100 grams per ton of feed.
Limitations

Feed continuously for 7 to 14 days. Do not administer to turkeys producing eggs for human consumption.

Indication
For control of infectious synovitis caused by M. synoviae susceptible to oxytetracycline.
Dosage
200 grams per ton of feed.
Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not administer to turkeys producing eggs for human consumption.

Swine

Indication
For treatment of bacterial enteritis caused by E. coli and Salmonella choleraesuis susceptible to oxytetracycline and treatment of bacterial pneumonia caused by P. multocida susceptible to oxytetracycline.
Dosage
10 milligrams per pound of body weight.
Limitations

Feed continuously for 7 to 14 days. 

Swine (Breeding)

Indication

For control and treatment of leptospirosis (reducing the incidence of abortion and shedding of leptospirae) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight.
Limitations

Feed continuously for not more than 14 days.  

Cattle (beef and non-lactating dairy: growing cattle over 400 pounds)

Indication

For the reduction of the incidence of liver abscesses.

Dosage

75 milligrams per head per day.

Limitations

Feed continuously.

Cattle (calves including veal calves, beef, and non-lactating dairy)

Indication

Treatment of bacterial enteritis caused by E. coli.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. In milk replacer or starter feed. Withdraw 0 days before slaughter. When used in milk replacers, the treatment claim (10 mg/lb) is limited to bacterial enteritis caused by E. coli only.

Indication

Treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline).

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Withdraw 0 days before slaughter.

Indication
For prevention and treatment of the early stages of shipping fever complex.
Dosage
0.5 - 2.0 grams per head per day in feed.
Limitations

Feed 3 to 5 days before and after arrival in feedlots. 

Sheep

Indication

For treatment of bacterial enteritis caused by E. coli and bacterial pneumonia caused by P. multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter.

Lobsters

Indication
For control of gaffkemia caused by Aerococcus viridans.
Dosage
1 gram per pound medicated feed.
Limitations

Administer as sole ration for 5 consecutive days. Withdraw medicated feed 30 days before harvesting lobsters.

Honey bees

Indication

Control of American Foulbrood caused by Bacillus larvae, and European foulbrood caused by Streptococcus pluton susceptible to oxytetracycline.

Dosage

200 milligrams per colony.

Limitations

Remove at least 6 weeks prior to main honey flow.

TM-100®D

SPL · SPL

FDA Structured Product Label

TM-50® TM-50® D TM-100® TM-100®D

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Phibro Animal Health Corp.
NADA
8804
Status
VFD
Form
Type A Medicated Article
Route
Oral
Species
Honey Bees • Breeding • No use class stated or implied • Beef • Calves • Dairy, non-lactating • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Lobster • Sheep, No Use Class Stated Or Implied
Composition / specifications
Type A medicated articles containing 50 grams oxytetracycline (from oxytetracycline quaternary salt) equivalent to oxytetracycline hydrochloride per pound

Chickens

Indication
For reduction of mortality due to air sacculitis (air-sac infection) caused by E. coli susceptible to oxytetracycline.
Dosage
500 grams per ton of feed.
Limitations

Feed continuously for 5 days. Do not administer to chickens producing eggs for human consumption. Withdraw 24 hours before slaughter. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues.

Indication
For control of chronic respiratory disease (CRD) and air sac infection caused by M. gallisepticum and Escherichia coli susceptible to oxytetracycline.
Dosage
400 grams per ton of feed.
Limitations

Feed continuously for 7 to 14 days. Do not administer to chickens producing eggs for human consumption. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues.

Indication
Control of infectious synovitis caused by Mycoplasma synoviae; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.
Dosage
100 - 200 grams per ton of feed.
Limitations

Feed continuously for 7 to 14 days. Do not administer to chickens producing eggs for human consumption. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues.

Turkeys

Indication
For control of complicating bacterial organisms associated with bluecomb (transmissible enteritis; coronaviral enteritis) susceptible to oxytetracycline.
Dosage
25 milligrams per pound of body weight.
Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not administer to turkeys producing eggs for human consumption.

Indication
For control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.
Dosage
100 grams per ton of feed.
Limitations

Feed continuously for 7 to 14 days. Do not administer to turkeys producing eggs for human consumption.

Indication
For control of infectious synovitis caused by M. synoviae susceptible to oxytetracycline.
Dosage
200 grams per ton of feed.
Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not administer to turkeys producing eggs for human consumption.

Swine

Indication
For treatment of bacterial enteritis caused by E. coli and Salmonella choleraesuis susceptible to oxytetracycline and treatment of bacterial pneumonia caused by P. multocida susceptible to oxytetracycline.
Dosage
10 milligrams per pound of body weight.
Limitations

Feed continuously for 7 to 14 days. 

Swine (Breeding)

Indication

For control and treatment of leptospirosis (reducing the incidence of abortion and shedding of leptospirae) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight.
Limitations

Feed continuously for not more than 14 days.  

Cattle (beef and non-lactating dairy: growing cattle over 400 pounds)

Indication

For the reduction of the incidence of liver abscesses.

Dosage

75 milligrams per head per day.

Limitations

Feed continuously.

Cattle (calves including veal calves, beef, and non-lactating dairy)

Indication

Treatment of bacterial enteritis caused by E. coli.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. In milk replacer or starter feed. Withdraw 0 days before slaughter. When used in milk replacers, the treatment claim (10 mg/lb) is limited to bacterial enteritis caused by E. coli only.

Indication

Treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline).

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Withdraw 0 days before slaughter.

Indication
For prevention and treatment of the early stages of shipping fever complex.
Dosage
0.5 - 2.0 grams per head per day in feed.
Limitations

Feed 3 to 5 days before and after arrival in feedlots. 

Sheep

Indication

For treatment of bacterial enteritis caused by E. coli and bacterial pneumonia caused by P. multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter.

Lobsters

Indication
For control of gaffkemia caused by Aerococcus viridans.
Dosage
1 gram per pound medicated feed.
Limitations

Administer as sole ration for 5 consecutive days. Withdraw medicated feed 30 days before harvesting lobsters.

Honey bees

Indication

Control of American Foulbrood caused by Bacillus larvae, and European foulbrood caused by Streptococcus pluton susceptible to oxytetracycline.

Dosage

200 milligrams per colony.

Limitations

Remove at least 6 weeks prior to main honey flow.

Oxytet® Soluble

SPL · SPL

FDA Structured Product Label

Oxytet® Soluble OXYMarine™

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Huvepharma EOOD
NADA
130-435
Status
RX
Form
Soluble Powder
Route
Immersion
Species
Fish, Finfish, Fry And Fingerlings
Composition / specifications
Each gram of soluble powder contains 366 milligrams (mg) of oxytetracycline hydrochloride.

Finfish

Indication
For skeletal marking of finfish fry and fingerlings.
Dosage
Immerse fish in a solution containing 200 to 700 mg oxytetracycline hydrochloride (buffered) per liter of water for 2 to 6 hours.

OXYMarine™

SPL · SPL

FDA Structured Product Label

Oxytet® Soluble OXYMarine™

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Huvepharma EOOD
NADA
130-435
Status
RX
Form
Soluble Powder
Route
Immersion
Species
Fish, Finfish, Fry And Fingerlings
Composition / specifications
Each gram of soluble powder contains 366 milligrams (mg) of oxytetracycline hydrochloride.

Finfish

Indication
For skeletal marking of finfish fry and fingerlings.
Dosage
Immerse fish in a solution containing 200 to 700 mg oxytetracycline hydrochloride (buffered) per liter of water for 2 to 6 hours.

Tetroxy® 25

SPL · SPL

FDA Structured Product Label

Tetroxy® 25

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Bimeda Animal Health Limited
ANADA
200-146
Status
RX
Form
Soluble Powder
Route
Oral
Species
Honey Bees • Breeding • No use class stated or implied • Beef • Calves • Dairy, females Under 20 months of age • Growing • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Sheep, No Use Class Stated Or Implied
Composition / specifications
Each 18.1 grams of powder contains 1 gram of oxytetracycline hydrochloride (packet: 6.4 oz; pails: 2 and 5 lb)

Chickens

Indication

Control of chronic respiratory disease (CRD) and air sac infections caused by Mycoplasma gallisepticum and E. coli susceptible to oxytetracycline; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage
400 to 800 milligrams per gallon of drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Indication

Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage

200 to 400 milligrams per gallon of drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Turkeys

Indication

Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage
400 milligrams per gallon of drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of oxytetracycline. Use as a sole source of drinking water. Do not use in birds producing eggs for human consumption. Withdraw 5 days prior to slaughter.

Indication

Control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.

Dosage

200 - 400 milligrams per gallon of drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of oxytetracycline. Use as a sole source of drinking water. Do not use in birds producing eggs for human consumption. Withdraw 5 days prior to slaughter.

Turkeys (growing)

Indication
Control of complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis) susceptible to oxytetracycline.
Dosage

25 milligrams per pound of body weight.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of oxytetracycline. Use as a sole source of drinking water. Do not use in birds producing eggs for human consumption. Withdraw 5 days prior to slaughter.

Swine

Indication

Control and treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight in drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Zero-day slaughter withdrawal in swine.

Swine (breeding stock)

Indication

Control and treatment of leptospirosis (reducing the incidence of abortions and shedding of leptospira) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Zero–day slaughter withdrawal in swine.

Cattle (calves, beef and nonlactating dairy)

Indication

Control and treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight in drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as sole source of oxytetracycline. Do not administer this product with milk or milk replacers. Administer 1 hour before or 2 hours after feeding milk or milk replacers. Withdraw 5 days prior to slaughter. A milk discard period has not been established for this product in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older.

Sheep

Indication

Control and treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight in drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Withdraw 5 days prior to slaughter.

Honey bees

Indication

Control of American foul brood caused by Paenibacillus larvae susceptible to oxytetracycline.

Dosage

200 milligrams per colony, administered via either an 1:1 sugar syrup (equal parts of sugar and water weight to weight) or dusting with a powdered sugar mixture.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. The drug is administered in 3 applications of sugar syrup or 3 dustings at 4- to 5- days intervals. The drug should be fed early in the spring or fall and consumed by the bees before main honey flow begins to avoid contamination of production honey. Remove at least 6 weeks prior to main honey flow. Dusting of uncapped brood cells has been reported to cause death of larval honey bees. Do not dust uncapped brood cells.

Tetroxy® 343

SPL · SPL

FDA Structured Product Label

Tetroxy® 343

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Bimeda Animal Health Limited
ANADA
200-247
Status
RX
Form
Powder
Route
Oral, Immersion
Species
Honey Bees • Fish, Finfish, Fry And Fingerlings • Breeding • No use class stated or implied • Beef • Calves • Dairy, females Under 20 months of age • Growing • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Sheep, No Use Class Stated Or Implied
Composition / specifications
Each 1.32 grams of powder contains 1 gram of OTC HCl (packet: 4.78 ounce and 9.6 ounce; pails 2 and 5 pounds)

Chickens

Indication

Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage
200 to 400 milligrams per gallon of drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Indication

Control of chronic respiratory disease (CRD) and air sac infections caused by Mycoplasma gallisepticum and E. coli susceptible to oxytetracycline; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage
400 to 800 milligrams per gallon of drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Turkeys

Indication

For the control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.

Dosage

200 – 400 milligrams per gallon of drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of oxytetracycline. Use as a sole source of drinking water. Do not use in birds producing eggs for human consumption. Withdraw 5 days before slaughter.

Indication

Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage
400 milligrams per gallon of drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of oxytetracycline. Use as a sole source of drinking water. Do not use in birds producing eggs for human consumption. Withdraw 5 days before slaughter.

Turkeys (growing)

Indication

Control of complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis) susceptible to oxytetracycline.

Dosage
25 milligrams per pound of body weight in drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of oxytetracycline. Use as a sole source of drinking water. Do not use in birds producing eggs for human consumption. Withdraw 5 days before slaughter.

Swine

Indication

Control and treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight in drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Zero-day slaughter withdrawal in swine.

Swine (breeding stock)

Indication

Control and treatment of leptospirosis (reducing the incidence of abortions and shedding of leptospira) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Zero–day slaughter withdrawal in swine.

Cattle (calves, beef, and nonlactating dairy)

Indication

Control and treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight in drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as sole source of oxytetracycline. Do not administer this product with milk or milk replacers. Administer 1 hour before or 2 hours after feeding milk or milk replacers. Withdraw 5 days prior to slaughter. A milk discard period has not been established for this product in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older.

Sheep

Indication

Control and treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight in drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Withdraw 5 days prior to slaughter.

Honey bees

Indication

Control of American foul brood caused by Paenibacillus larvae susceptible to oxytetracycline.

Dosage

200 milligrams per colony, administered via either a 1:1 sugar syrup (equal parts of sugar and water weight to weight) or dusting with a powdered sugar mixture.

Finfish fry and fingerlings

Indication
For skeletal marking of finfish fry and fingerlings.
Dosage

Immerse fish in a solution containing 200 to 700 mg oxytetracycline hydrochloride (buffered) per liter of water for 2 to 6 hours.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Tetroxy® Aquatic

SPL · SPL

FDA Structured Product Label

Tetroxy® Aquatic

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Bimeda Animal Health Limited
ANADA
200-460
Status
RX
Form
Liquid (Solution)
Route
Immersion
Species
Fish, Finfish, Fry And Fingerlings
Composition / specifications
Each 2.73 grams of powder contains 1 gram of OTC HCl (packets: 2.46 and 9.87 ounce; pail: 3.09 pound). Each gram of powder contains 366 milligrams (mg) of oxytetracycline hydrochloride.

Finfish

Indication
For skeletal marking of finfish fry and fingerlings
Dosage

Immerse fish in a solution containing 200 to 700 mgoxytetracycline hydrochloride (buffered) per liter of water for 2 to 6 hours.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian

AGRIMYCIN®-343

SPL · SPL

FDA Structured Product Label

AGRIMYCIN®-343

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Huvepharma EOOD
ANADA
200-066
Status
RX
Form
Soluble Powder
Route
Oral
Species
Breeding • No use class stated or implied • Growing • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption
Composition / specifications
4.78 oz. (135.5 g) pouch: each packet contains 102.4 grams of oxytetracycline hydrochloride. 5 lb. (2.27 kg) pail: each pail contains 1.715 kilograms of oxytetracycline hydrochloride. 3.09 lb. (1400 g) pouch: each packet contains 512 grams of oxytetracycline hydrochloride. 9.87 oz. (280 g) packet: each packet contains 102.4 grams of oxytetracycline hydrochloride

Chickens

Indication

For the control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage

Administer 200 to 400 milligrams of powder per gallon of drinking water.

Limitations

Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption. Use as the sole source of oxytetracycline. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Indication

For the control of chronic respiratory disease (CRD) and air sac infections caused by Mycoplasma gallisepticum and E. coli susceptible to oxytetracycline; for the control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

Administer 400 to 800 milligrams of powder per gallon of drinking water.

Limitations

Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption. Use as the sole source of oxytetracycline. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Turkeys

Indication

For the control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.

Dosage

Administer 200 to 400 milligrams of powder per gallon of drinking water.

Limitations

Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption. Use as the sole source of oxytetracycline. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Indication

For the control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage

Administer 400 milligrams of powder per gallon of drinking water.

Limitations

Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption. Use as the sole source of oxytetracycline. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Turkeys (growing)

Indication

For the control of complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis) susceptible to oxytetracycline.

Dosage

Administer 25 milligrams per pound of body weight in drinking water.

Limitations

Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption. Use as the sole source of oxytetracycline. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Swine

Indication

For the control and treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

Administer 10 milligrams per pound of body weight daily in drinking water.

Limitations

Prepare a fresh solution daily. Use as the sole source of oxytetracycline. Administer up to 5 days; do not use for more than 5 consecutive days. Use as sole source of drinking water. Do not mix this product directly with milk or milk replacers. Administer one hour before or two hours after feeding milk or milk replacers. Withdraw zero days prior to slaughter. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Swine (breeding stock)

Indication

For the control and treatment of leptospirosis (reducing the incidence of abortions and shedding of leptospira) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage

Administer 10 milligrams per pound of body weight daily in drinking water.

Limitations

Prepare a fresh solution daily. Use as the sole source of oxytetracycline. Administer up to 5 days; do not use for more than 5 consecutive days. Use as sole source of drinking water. Do not mix this product directly with milk or milk replacers. Administer one hour before or two hours after feeding milk or milk replacers. Withdraw zero days prior to slaughter. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

OXY WS™

SPL · SPL

FDA Structured Product Label

OXY WS™

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Phibro Animal Health Corp.
NADA
38200
Status
RX
Form
Soluble Powder
Route
Oral
Species
Growing • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption
Composition / specifications
Each 4.2 gram of powder contains 1 gram of oxytetracycline hydrochloride.

Chickens

Indication

Control of chronic respiratory disease (CRD) and air sac infections caused by Mycoplasma gallisepticum and E. coli and fowl cholera caused by Pasteurella multocida.

Dosage

400 to 800 milligrams per gallon of drinking water. 

Limitations

Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Indication
Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.
Dosage

200 to 400 milligrams per gallon of drinking water. 

Limitations

Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Turkeys

Indication
Control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.
Dosage

200 to 400 milligrams per gallon of drinking water. 

Limitations

Administer for 7 to 14 days; do not slaughter for food within 4 days of treatment; not for use in turkeys producing eggs for human consumption; prepare a fresh solution daily; use as the sole source of tetracycline.

Indication
Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.
Dosage

400 milligrams per gallon of drinking water. 

Limitations

Administer for 7 to 14 days; do not slaughter for food within 4 days of treatment; not for use in turkeys producing eggs for human consumption; prepare a fresh solution daily; use as the sole source of tetracycline.

Indication

Control of complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis).

Dosage

25 mg/lb of body weight per day in drinking water.

Limitations

Administer for 7 to 14 days; do not slaughter for food within 4 days of treatment; not for use in turkeys producing eggs for human consumption; prepare a fresh solution daily; use as the sole source of tetracycline.

Pennox 343®

SPL · SPL

FDA Structured Product Label

Pennox 343®

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Pharmgate Inc.
ANADA
200-026
Status
RX
Form
Soluble Powder
Route
Immersion, Oral
Species
Honey Bees • Fish, Finfish, Fry And Fingerlings • Breeding • No use class stated or implied • Beef • Calves • Dairy, females Under 20 months of age • Growing • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Sheep, No Use Class Stated Or Implied
Composition / specifications
Each 677.5 gram packet contains 512 grams of oxytetracycline hydrochloride (OTC HCL)(packet 23.9 oz).

Chickens

Indication
Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.
Dosage
200 to 400 milligrams per gallon of drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Indication
Control of chronic respiratory disease (CRD) and air sac infections caused by Mycoplasma gallisepticum and E. coli susceptible to oxytetracycline; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.
Dosage
400 to 800 milligrams per gallon of drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Turkeys

Indication

Control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.

Dosage
200 - 400 milligrams per gallon of drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of oxytetracycline. Use as a sole source of drinking water. Do not use in birds producing eggs for human consumption. Zero day slaughter withdrawal in turkeys.

Indication
Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.
Dosage
400 milligrams per gallon of drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of oxytetracycline. Use as a sole source of drinking water. Do not use in birds producing eggs for human consumption. Zero day slaughter withdrawal in turkeys.

Turkeys (growing)

Indication
Control of complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis) susceptible to oxytetracycline.
Dosage

25 milligrams per pound of body weight.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of oxytetracycline. Use as a sole source of drinking water. Do not use in birds producing eggs for human consumption. Zero day slaughter withdrawal in turkeys.

Swine

Indication

Control and treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight daily in drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Administer up to 5 days. Do not use for more than 5 consecutive days. Zero day slaughter withdrawal in swine.

Cattle (calves, beef, and nonlactating dairy)

Indication
Control and treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline.
Dosage
10 milligrams per pound of body weight daily in drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer up to 5 days. Do not use for more than 5 consecutive days. Use as sole source of oxytetracycline. Do not administer this product with milk or milk replacers. Administer 1 hour before or 2 hours after feeding milk or milk replacers. Withdraw 5 days prior to slaughter. A milk discard period has not been established for this product in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older.

Swine (breeding stock)

Indication

Control and treatment of leptospirosis (reducing the incidence of abortions and shedding of leptospira) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Administer up to 5 days. Do not use for more than 5 consecutive days. Zero day slaughter withdrawal in swine.

Sheep

Indication
Control and treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline.
Dosage
10 milligrams per pound of body weight in drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer up to 5 days. Do not use for more than 5 consecutive days. Use as a sole source of oxytetracycline. Withdraw 5 days prior to slaughter.

Honey Bees

Indication

Control of American foul brood caused by Paenibacillus larvae susceptible to oxytetracycline.

Dosage
200 milligrams per colony, administered via either a 1:1 sugar syrup (equal parts of sugar and water weight to weight) or dusting with a powdered sugar mixture.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. The drug is administered in 3 applications of sugar syrup or 3 dustings at 4- to 5- days intervals. The drug should be fed early in the spring or fall and consumed by the bees before main honey flow begins to avoid contamination of production honey. Remove at least 6 weeks prior to main honey flow. Dusting of uncapped brood cells has been reported to cause death of larval honey bees. Do not dust uncapped brood cells.

Finfish fry and fingerlings

Indication

For skeletal marking of finfish fry and fingerlings.

Dosage

Immerse fish in a solution containing 200 to 700 mg oxytetracycline hydrochloride (buffered) per liter of water for 2 to 6 hours.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. For skeletal marking of finfish fry and fingerlings.

Geomycin 200

SPL · SPL

FDA Structured Product Label

Geomycin 200

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Pliva, d. d.
ANADA
200-232
Status
OTC
Form
Liquid (Solution)
Route
Subcutaneous, Intramuscular, Intravenous
Species
Cattle, Dairy, Not Lactating • Swine, No Use Class Stated Or Implied • Swine, Sows With Litters Or About To Farrow • Cattle, Beef
Composition / specifications
200 milligrams/milliliter

Sows

Indication
As an aid in control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by E. coli.
Dosage
3 milligrams per pound of body weight intramuscularly once.
Limitations
Administer intramuscularly. Do not inject more than 5 mL per site in adult swine. Discontinue treatment at least 28 days prior to slaughter.

Swine

Indication
Where re-treatment for pneumonia is impractical.
Dosage
9 milligrams per pound of body weight as a single dosage.
Limitations
Administer intramuscularly. Do not inject more than 5 mL per site in adult swine. Discontinue treatment at least 28 days prior to slaughter.
Indication
For treatment of bacterial enteritis (scours, colibacillosis) caused by E. coli, pneumonia caused by Pasteurella multocida, and leptospirosis caused by Leptospira pomona.
Dosage
3 to 5 milligrams of oxytetracycline per pound of body weight per day.
Limitations
Administer intramuscularly. Do not inject more than 5 mL per site in adult swine. Discontinue treatment at least 28 days prior to slaughter.

Cattle (beef,dairy excluding lactating animals, and calves, including preruminating veal calves)

Indication
Where retreatment of calves and yearlings for bacterial pneumonia is impractical, for treatment of infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis, or where retreatment for anaplasmosis is impractical.
Dosage
9 milligrams per pound of body weight intramuscularly or subcutaneously as a single dose.
Limitations
Administer intramuscularly or intravenously. Exceeding the highest recommended level of drug per pound of bodyweight per day, administering more than the recommended number of treatments, and/or exceeding 10 mL intramuscularly or subcutaneously per injection site may result in antibiotic residues beyond the withdrawal time. Rapid intravenous administration in cattle may result in animal collapse. Oxytetracycline should be administered intravenously slowly over a period of at least 5 minutes. Discontinue treatment at least 28 days prior to slaughter. Not for use in lactating dairy animals. Federal law restricts this drug to use by or on the order of a licensed veterinarian.
Indication
For treatment of anaplasmosis, severe foot-rot and advanced cases of other indicated diseases.
Dosage
5 milligrams per pound of body weight per day.
Limitations
Administer intramuscularly, subcutaneously, or intravenously. Exceeding the highest recommended level of drug per pound of bodyweight per day, administering more than the recommended number of treatments, and/or exceeding 10 mL intramuscularly or subcutaneously per injection site may result in antibiotic residues beyond the withdrawal time. Rapid intravenous administration in cattle may result in animal collapse. Oxytetracycline should be administered intravenously slowly over a period of at least 5 minutes. Discontinue treatment at least 28 days prior to slaughter. Not for use in lactating dairy animals.
Indication
For treatment of pneumonia and shipping fever complex associated with Pasteurella species and Haemophilus species, foot-rot and diphtheria caused by Fusobacterium necrophorum, bacterial enteritis (scours) caused by Escherichia coli, wooden tongue caused by Actinobacillus lignieresii, leptospirosis caused by Leptospira pomona, wound infections and acute metritis caused by Staphylococcus species and Streptococcus species, and anthrax caused by Bacillus anthracis.
Dosage
3 to 5 milligrams of oxytetracycline per pound of body weight per day.
Limitations
Administer intramuscularly, subcutaneously, or intravenously. Exceeding the highest recommended level of drug per pound of bodyweight per day, administering more than the recommended number of treatments, and/or exceeding 10 mL intramuscularly or subcutaneously per injection site may result in antibiotic residues beyond the withdrawal time. Rapid intravenous administration in cattle may result in animal collapse. Oxytetracycline should be administered intravenously slowly over a period of at least 5 minutes. Discontinue treatment at least 28 days prior to slaughter. Not for use in lactating dairy animals. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Liquamycin® Injectable

SPL · SPL

FDA Structured Product Label

Liquamycin® Injectable Terramycin® Injectable

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Zoetis Inc.
NADA
8769
Status
RX
Form
Liquid (Solution)
Route
Intravenous, Intramuscular, Subcutaneous
Species
No use class stated or implied • Sows with litters or about to farrow • Beef • Dairy, non-lactating • Breeders not laying eggs for human consumption • Broilers not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption
Composition / specifications
The drug contains 50 milligrams of oxytetracycline hydrochloride in each milliliter of sterile solution.

Cattle (beef and nonlactating dairy)

Indication
It is used for the treatment of pneumonia and shipping fever complex associated with Pasteurella species and Hemophilus species; foot-rot and diphtheria caused by Spherophorus necrophorus; bacterial enteritis (scours) caused by Escherichia coli; wooden tongue caused by Actinobacillus lignieresi; leptospirosis caused by Leptospira pomona; wound infections and acute metritis caused by staphylococcal and streptococcal organisms.
Dosage
Administer by intravenous or intramuscular injection at 3 to 5 milligrams of oxytetracycline per pound of body weight per day. In the treatment of severe foot-rot and severe forms of the indicated diseases, a dosage level of 5 milligrams per pound of body weight per day is recommended. If the labeling of the drug bears the statement ``Federal law restricts this drug to use by or on the order of a licensed veterinarian,'' it may include additional directions for use in beef cattle and nonlactating dairy cattle for the treatment of anaplasmosis caused by Anaplasma marginale and anthrax caused by Bacillus anthracis in which case the drug is given at 3 to 5 milligrams of oxytetracycline per pound of body weight per day for anthrax, and at 5 milligrams per pound of body weight per day for anaplasmosis.
Limitations
Treatment of all diseases should be instituted early. Treatment should continue for 24 to 48 hours beyond the remission of disease symptoms, but not exceed a total of 4 consecutive days. If no improvement is noted within 24 to 48 hours, diagnosis and therapy should be reevaluated. When injecting intramuscularly in adult livestock, do not inject more than 10 milliliters at any one site. The volume administered per injection site should be reduced according to age and body size so that 1 or 2 milliliters are injected in smaller animals such as small calves. Intravenous administration is recommended in cattle when daily dosage exceeds 50 milliliters. Treatment must be discontinued at least 22 days prior to slaughter for cattle. When administered intramuscularly to animals within 30 days of slaughter, muscle discoloration may necessitate trimming of the injection site(s) and surrounding tissues during the dressing procedure. Not for use in lactating dairy animals.

Swine

Indication
It is used for the treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli; pneumonia caused by Pasteurella multocida; and leptospirosis caused by Leptospira pomona.
Dosage
Administer by intramuscular injection at 3 to 5 milligrams of oxytetracycline per pound of body weight per day to swine.
Limitations
Treatment of all diseases should be instituted early. Treatment should continue for 24 to 48 hours beyond the remission of disease symptoms, but not exceed a total of 4 consecutive days. If no improvement is noted within 24 to 48 hours, diagnosis and therapy should be reevaluated. When injecting intramuscularly in adult livestock, do not inject more than 10 milliliters at any one site. The volume administered per injection site should be reduced according to age and body size so that 1 or 2 milliliters are injected in smaller animals such as young pigs. Treatment must be discontinued at least 22 days prior to slaughter for swine. When administered intramuscularly to animals within 30 days of slaughter, muscle discoloration may necessitate trimming of the injection site(s) and surrounding tissues during the dressing procedure.

Swine (sows about to farrow or just farrowed).

Indication
Administered to sows as an aid in the control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.
Dosage
Administered to sows at 3 milligrams of oxytetracycline per pound of body weight approximately 8 hours before farrowing or immediately after farrowing. Administer intramuscularly.
Limitations
Treatment of all diseases should be instituted early. Treatment should continue for 24 to 48 hours beyond the remission of disease symptoms, but not exceed a total of 4 consecutive days. If no improvement is noted within 24 to 48 hours, diagnosis and therapy should be reevaluated. When injecting intramuscularly in adult livestock, do not inject more than 10 milliliters at any one site. The volume administered per injection site should be reduced according to age and body size so that 1 or 2 milliliters are injected in smaller animals such as young pigs. Treatment must be discontinued at least 22 days prior to slaughter for swine. When administered intramuscularly to animals within 30 days of slaughter, muscle discoloration may necessitate trimming of the injection site(s) and surrounding tissues during the dressing procedure.

Chickens (broilers and breeding chickens)

Indication
It is used for the treatment of air sacculitis (air-sac disease chronic respiratory disease) caused by Mycoplasma gallisepticum and Escherichia coli; fowl cholera caused by Pasteurella multocida; infectious sinusitis caused by Mycoplasma gallisepticum; and infectious synovitis caused by Mycoplasma synoviae.
Dosage
Administered subcutaneously to chickens 1 day to 2 weeks of age at 6.25 milligrams of oxytetracycline per bird per day diluted with 1 part of the drug to 3 parts of sterile water; to chickens 2 to 4 weeks of age using the same diluted product at 12.5 milligrams of oxytetracycline per bird; to chickens 4 to 8 weeks of age without dilution at 25 milligrams of oxytetracycline per bird; to chickens 8 weeks of age (broilers and light pullets) at 50 milligrams of oxytetracycline per bird; to adult chickens at 100 milligrams of oxytetracycline per bird.
Limitations
Treatment of all diseases should be instituted early. Treatment should continue for 24 to 48 hours beyond the remission of disease symptoms, but not exceed a total of 4 consecutive days. If no improvement is noted within 24 to 48 hours, diagnosis and therapy should be reevaluated. Treatment must be discontinued at least 5 days prior to slaughter for chickens. Do not administer to laying hens unless the eggs are used for hatching only.

Turkeys

Indication
It is used for the treatment of air sacculitis (air-sac disease chronic respiratory disease) caused by Mycoplasma gallisepticum and Escherichia coli; fowl cholera caused by Pasteurella multocida; infectious sinusitis caused by Mycoplasma gallisepticum; and infectious synovitis caused by Mycoplasma synoviae.
Dosage
Administered subcutaneously to turkeys 1 day to 2 weeks of age and 2 to 4 weeks of age at the same dosage as chickens; to turkeys 4 to 6 weeks of age at 50 milligrams of oxytetracycline as the undiluted product per bird; to turkeys 6 to 9 weeks of age at 100 milligrams of oxytetracycline per bird; to turkeys 9 to 12 weeks of age at 150 milligrams of oxytetracycline per bird; to turkeys 12 weeks of age and older at 200 milligrams of oxytetracycline per bird. In light turkey breeds, no more than 25 milligrams per pound of body weight is administered. For the treatment of infectious sinusitis in turkeys, 1/4 to 1/2 milliliter of the drug is injected directly into each swollen sinus depending upon the age of the bird and the severity of the condition. At the time that the sinuses are treated, the drug should also be administered subcutaneously to the birds according to the dosage schedule stated above for chickens and turkeys. If refilling of the sinuses occurs, the treatment may be repeated in 5 to 7 days.
Limitations
Treatment of all diseases should be instituted early. Treatment should continue for 24 to 48 hours beyond the remission of disease symptoms, but not exceed a total of 4 consecutive days. If no improvement is noted within 24 to 48 hours, diagnosis and therapy should be reevaluated. Treatment must be discontinued at least 5 days prior to slaughter for turkeys. Do not administer to laying hens unless the eggs are used for hatching only.

Terramycin® Injectable

SPL · SPL

FDA Structured Product Label

Liquamycin® Injectable Terramycin® Injectable

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Zoetis Inc.
NADA
8769
Status
RX
Form
Liquid (Solution)
Route
Intravenous, Intramuscular, Subcutaneous
Species
No use class stated or implied • Sows with litters or about to farrow • Beef • Dairy, non-lactating • Breeders not laying eggs for human consumption • Broilers not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption
Composition / specifications
The drug contains 50 milligrams of oxytetracycline hydrochloride in each milliliter of sterile solution.

Cattle (beef and nonlactating dairy)

Indication
It is used for the treatment of pneumonia and shipping fever complex associated with Pasteurella species and Hemophilus species; foot-rot and diphtheria caused by Spherophorus necrophorus; bacterial enteritis (scours) caused by Escherichia coli; wooden tongue caused by Actinobacillus lignieresi; leptospirosis caused by Leptospira pomona; wound infections and acute metritis caused by staphylococcal and streptococcal organisms.
Dosage
Administer by intravenous or intramuscular injection at 3 to 5 milligrams of oxytetracycline per pound of body weight per day. In the treatment of severe foot-rot and severe forms of the indicated diseases, a dosage level of 5 milligrams per pound of body weight per day is recommended. If the labeling of the drug bears the statement ``Federal law restricts this drug to use by or on the order of a licensed veterinarian,'' it may include additional directions for use in beef cattle and nonlactating dairy cattle for the treatment of anaplasmosis caused by Anaplasma marginale and anthrax caused by Bacillus anthracis in which case the drug is given at 3 to 5 milligrams of oxytetracycline per pound of body weight per day for anthrax, and at 5 milligrams per pound of body weight per day for anaplasmosis.
Limitations
Treatment of all diseases should be instituted early. Treatment should continue for 24 to 48 hours beyond the remission of disease symptoms, but not exceed a total of 4 consecutive days. If no improvement is noted within 24 to 48 hours, diagnosis and therapy should be reevaluated. When injecting intramuscularly in adult livestock, do not inject more than 10 milliliters at any one site. The volume administered per injection site should be reduced according to age and body size so that 1 or 2 milliliters are injected in smaller animals such as small calves. Intravenous administration is recommended in cattle when daily dosage exceeds 50 milliliters. Treatment must be discontinued at least 22 days prior to slaughter for cattle. When administered intramuscularly to animals within 30 days of slaughter, muscle discoloration may necessitate trimming of the injection site(s) and surrounding tissues during the dressing procedure. Not for use in lactating dairy animals.

Swine

Indication
It is used for the treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli; pneumonia caused by Pasteurella multocida; and leptospirosis caused by Leptospira pomona.
Dosage
Administer by intramuscular injection at 3 to 5 milligrams of oxytetracycline per pound of body weight per day to swine.
Limitations
Treatment of all diseases should be instituted early. Treatment should continue for 24 to 48 hours beyond the remission of disease symptoms, but not exceed a total of 4 consecutive days. If no improvement is noted within 24 to 48 hours, diagnosis and therapy should be reevaluated. When injecting intramuscularly in adult livestock, do not inject more than 10 milliliters at any one site. The volume administered per injection site should be reduced according to age and body size so that 1 or 2 milliliters are injected in smaller animals such as young pigs. Treatment must be discontinued at least 22 days prior to slaughter for swine. When administered intramuscularly to animals within 30 days of slaughter, muscle discoloration may necessitate trimming of the injection site(s) and surrounding tissues during the dressing procedure.

Swine (sows about to farrow or just farrowed).

Indication
Administered to sows as an aid in the control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.
Dosage
Administered to sows at 3 milligrams of oxytetracycline per pound of body weight approximately 8 hours before farrowing or immediately after farrowing. Administer intramuscularly.
Limitations
Treatment of all diseases should be instituted early. Treatment should continue for 24 to 48 hours beyond the remission of disease symptoms, but not exceed a total of 4 consecutive days. If no improvement is noted within 24 to 48 hours, diagnosis and therapy should be reevaluated. When injecting intramuscularly in adult livestock, do not inject more than 10 milliliters at any one site. The volume administered per injection site should be reduced according to age and body size so that 1 or 2 milliliters are injected in smaller animals such as young pigs. Treatment must be discontinued at least 22 days prior to slaughter for swine. When administered intramuscularly to animals within 30 days of slaughter, muscle discoloration may necessitate trimming of the injection site(s) and surrounding tissues during the dressing procedure.

Chickens (broilers and breeding chickens)

Indication
It is used for the treatment of air sacculitis (air-sac disease chronic respiratory disease) caused by Mycoplasma gallisepticum and Escherichia coli; fowl cholera caused by Pasteurella multocida; infectious sinusitis caused by Mycoplasma gallisepticum; and infectious synovitis caused by Mycoplasma synoviae.
Dosage
Administered subcutaneously to chickens 1 day to 2 weeks of age at 6.25 milligrams of oxytetracycline per bird per day diluted with 1 part of the drug to 3 parts of sterile water; to chickens 2 to 4 weeks of age using the same diluted product at 12.5 milligrams of oxytetracycline per bird; to chickens 4 to 8 weeks of age without dilution at 25 milligrams of oxytetracycline per bird; to chickens 8 weeks of age (broilers and light pullets) at 50 milligrams of oxytetracycline per bird; to adult chickens at 100 milligrams of oxytetracycline per bird.
Limitations
Treatment of all diseases should be instituted early. Treatment should continue for 24 to 48 hours beyond the remission of disease symptoms, but not exceed a total of 4 consecutive days. If no improvement is noted within 24 to 48 hours, diagnosis and therapy should be reevaluated. Treatment must be discontinued at least 5 days prior to slaughter for chickens. Do not administer to laying hens unless the eggs are used for hatching only.

Turkeys

Indication
It is used for the treatment of air sacculitis (air-sac disease chronic respiratory disease) caused by Mycoplasma gallisepticum and Escherichia coli; fowl cholera caused by Pasteurella multocida; infectious sinusitis caused by Mycoplasma gallisepticum; and infectious synovitis caused by Mycoplasma synoviae.
Dosage
Administered subcutaneously to turkeys 1 day to 2 weeks of age and 2 to 4 weeks of age at the same dosage as chickens; to turkeys 4 to 6 weeks of age at 50 milligrams of oxytetracycline as the undiluted product per bird; to turkeys 6 to 9 weeks of age at 100 milligrams of oxytetracycline per bird; to turkeys 9 to 12 weeks of age at 150 milligrams of oxytetracycline per bird; to turkeys 12 weeks of age and older at 200 milligrams of oxytetracycline per bird. In light turkey breeds, no more than 25 milligrams per pound of body weight is administered. For the treatment of infectious sinusitis in turkeys, 1/4 to 1/2 milliliter of the drug is injected directly into each swollen sinus depending upon the age of the bird and the severity of the condition. At the time that the sinuses are treated, the drug should also be administered subcutaneously to the birds according to the dosage schedule stated above for chickens and turkeys. If refilling of the sinuses occurs, the treatment may be repeated in 5 to 7 days.
Limitations
Treatment of all diseases should be instituted early. Treatment should continue for 24 to 48 hours beyond the remission of disease symptoms, but not exceed a total of 4 consecutive days. If no improvement is noted within 24 to 48 hours, diagnosis and therapy should be reevaluated. Treatment must be discontinued at least 5 days prior to slaughter for turkeys. Do not administer to laying hens unless the eggs are used for hatching only.

Liquimast Solution for Mastitis

SPL · SPL

This source does not expose a safe inline preview. Use the original source link for the full document.

Oxytetracycline Hydrochloride Soluble Powder

SPL · SPL

FDA Structured Product Label

Oxytetracycline Hydrochloride Soluble Powder

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Vetoquinol N.-A., Inc.
ANADA
200-305
Status
OTC
Form
Liquid (Solution)
Route
Oral
Species
Swine, Breeding Swine • Swine, No Use Class Stated Or Implied • Turkey, Growing • Turkey, Not Laying Eggs For Human Consumption • Chicken, Not Laying Eggs For Human Consumption
Composition / specifications
The drug is a soluble powder distributed in packets (9.87oz and 19.47oz) or pails (5lb). Each 2.73 grams of powder contains 1 gram of oxytetracycline hydrochloride.

Swine (breeding stock)

Indication
Control and treatment of leptospirosis (reducing the incidence of abortions and shedding of leptospira) caused by Leptospira pomona susceptible to oxytetracycline.
Dosage
10 milligrams per pound of body weight daily in drinking water.
Limitations
Prepare a fresh solution daily. Use as sole source of OTC. Administer up to 5 days. Do not use for more than 5 consecutive days.

Turkeys (growing)

Indication
Control of complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis) susceptible to oxytetracycline.
Dosage
25 milligrams per pound of body weight in drinking water.
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Swine

Indication
Control and treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.
Dosage
10 milligrams per pound of body weight daily in drinking water.
Limitations
Prepare a fresh solution daily. Use as sole source of OTC. Administer up to 5 days. Do not use for more than 5 consecutive days.

Chickens

Indication
Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.
Dosage
200 to 400 milligrams per gallon of drinking water.
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.
Indication
Control of chronic respiratory disease (CRD) and air sac infections caused by Mycoplasma gallisepticum and E. coli susceptible to oxytetracycline; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.
Dosage
400 to 800 milligrams per gallon of drinking water.
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Turkeys

Indication
Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.
Dosage
400 milligrams per gallon of drinking water.
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.
Indication
Control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.
Dosage
200 to 400 milligrams per gallon of drinking water.
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Oxytetracycline Premix

SPL · SPL

This source does not expose a safe inline preview. Use the original source link for the full document.

Purina® Mix-R-Mycin Concentrate

SPL · SPL

This source does not expose a safe inline preview. Use the original source link for the full document.

Terramycin® Egg Formula

SPL · SPL

This source does not expose a safe inline preview. Use the original source link for the full document.

Terramycin® Premix

SPL · SPL

FDA Structured Product Label

Terramycin® Premix

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Pfizer, Inc.
NADA
103-758
Status
OTC
Form
Medicated Feed
Route
Oral
Species
Chicken, Broilers
Composition / specifications
Type A medicated articles: 10, 20, 30, 40, 50, 100, and 200 grams per pound.

Chickens (broilers)

Indication
As an aid in the reduction of mortality due to air-sacculitis (air-sac-infection) caused by Escherichia coli sensitive to oxytetracycline.
Dosage
500 grams per ton of feed.
Limitations
Feed for 5 days as sole ration. Treat at first clinical signs of disease. Do not feed to laying hens. Withdraw 24 hours prior to slaughter.

Terramycin® Vet Capsules

SPL · SPL

FDA Structured Product Label

Terramycin® Vet Capsules

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
Zoetis Inc.
NADA
7879
Status
RX
Form
Capsule
Route
Oral
Species
Dog, No Use Class Stated Or Implied • Cat, No Use Class Stated Or Implied
Composition / specifications
The drug is in capsule form with each capsule containing 125 or 250 milligrams of oxytetracycline hydrochloride. Oxytetracycline is the antibiotic substance produced by growth of Streptomyces rimosus or the same antibiotic substance produced by any other means.

Dogs

Indication
It is used in dogs for the treatment of bacterial pneumonia caused by Brucella bronchiseptica, tonsillitis caused by Streptococcus hemolyticus, bacterial enteritis caused by Escherichia coli, urinary tract infections caused by Escherichia coli, and wound infections caused by Staphylococcus aureus. The drug can be used for continuation of compatible antibiotic therapy following parenteral oxytetracycline administration where rapidly attained, sustained antibiotic blood levels are required. The duration of treatment required to obtain favorable response will depend to some extent on the severity and degree of involvement and the susceptibility of the infectious agent. Clinical response to antibiotic therapy usually occurs within 48 to 72 hours. If improvement is not observed within that period, the diagnosis and course of treatment should be reconsidered. To assure adequate treatment, administration of the drug should continue for at least 48 hours following favorable clinical response.
Dosage
The drug is administered orally to dogs at a dosage level of 25- 50 milligrams per pound of body weight per day in divided doses at 12-hour intervals.
Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Cats

Indication
It is used in cats for the treatment of bacterial pneumonia caused by Brucella bronchiseptica, tonsillitis caused by Streptococcus hemolyticus, bacterial enteritis caused by Escherichia coli, urinary tract infections caused by Escherichia coli, and wound infections caused by Staphylococcus aureus. The drug can be used for continuation of compatible antibiotic therapy following parenteral oxytetracycline administration where rapidly attained, sustained antibiotic blood levels are required. The duration of treatment required to obtain favorable response will depend to some extent on the severity and degree of involvement and the susceptibility of the infectious agent. Clinical response to antibiotic therapy usually occurs within 48 to 72 hours. If improvement is not observed within that period, the diagnosis and course of treatment should be reconsidered. To assure adequate treatment, administration of the drug should continue for at least 48 hours following favorable clinical response.
Dosage
The drug is administered orally to cats at a dosage level of 25- 50 milligrams per pound of body weight per day in divided doses at 12-hour intervals.
Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian.

TM®-10 Premix

SPL · SPL

This source does not expose a safe inline preview. Use the original source link for the full document.

TM®-5 Antibiotic Feed Supplement

SPL · SPL

This source does not expose a safe inline preview. Use the original source link for the full document.

Oxytetracycline Dihydrate SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Oxytetracycline Dihydrate. Use the source link for the full official labeling record.

Oxytetracycline Hydrochloride SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Oxytetracycline Hydrochloride. Use the source link for the full official labeling record.

Oxytetracycline HCL SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Oxytetracycline HCL. Use the source link for the full official labeling record.

TERRA-VET 200 SPL

SPL · Structured Product Label

FDA Structured Product Label XML for TERRA-VET 200. Use the source link for the full official labeling record.

Terramycin Scours SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Terramycin Scours. Use the source link for the full official labeling record.

Pennox 343 SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Pennox 343. Use the source link for the full official labeling record.

VETRIMYCIN 200 SPL

SPL · Structured Product Label

FDA Structured Product Label XML for VETRIMYCIN 200. Use the source link for the full official labeling record.

Bio-Mycin 200 SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Bio-Mycin 200. Use the source link for the full official labeling record.

Vetrimycin 200 SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Vetrimycin 200. Use the source link for the full official labeling record.

Liquamycin LA-200 SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Liquamycin LA-200. Use the source link for the full official labeling record.

Tetroxy 343 SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Tetroxy 343. Use the source link for the full official labeling record.

Noromycin 300 LA SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Noromycin 300 LA. Use the source link for the full official labeling record.

Oxytetracycline 200 SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Oxytetracycline 200. Use the source link for the full official labeling record.

Tetroxy HCA SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Tetroxy HCA. Use the source link for the full official labeling record.

Oxytet Soluble SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Oxytet Soluble. Use the source link for the full official labeling record.

Terra-Vet 200 SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Terra-Vet 200. Use the source link for the full official labeling record.

AGRIMYCIN 200 SPL

SPL · Structured Product Label

FDA Structured Product Label XML for AGRIMYCIN 200. Use the source link for the full official labeling record.

Terramycin 200 Granular SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Terramycin 200 Granular. Use the source link for the full official labeling record.

Terramycin 100 SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Terramycin 100. Use the source link for the full official labeling record.

Pennox 100 Hi-Flo SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Pennox 100 Hi-Flo. Use the source link for the full official labeling record.

Pennox 50 SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Pennox 50. Use the source link for the full official labeling record.

Terramycin 50 SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Terramycin 50. Use the source link for the full official labeling record.

Terramycin 100 MR SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Terramycin 100 MR. Use the source link for the full official labeling record.

Terramycin 200 SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Terramycin 200. Use the source link for the full official labeling record.

AX Pharmaceutical Corp SPL

SPL · Structured Product Label

FDA Structured Product Label XML for AX Pharmaceutical Corp. Use the source link for the full official labeling record.

Oxytetracycline Hydrochloride SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Oxytetracycline Hydrochloride. Use the source link for the full official labeling record.

UCM539429.pdf

FOI · FOI

FOI Summary sN 008-622 Approved December 30, 2019.pdf

FOI · FOI

ucm049519.pdf

FOI · FOI

ucm049517.pdf

FOI · FOI

UCM523939.pdf

FOI · FOI

ucm079545.pdf

FOI · FOI

ucm079541.pdf

FOI · FOI

N095143_Org_5_30_96.pdf

FOI · FOI

FOI Summary oA 200-537 Approved May 30, 2019.pdf

FOI · FOI

A-200117-Q-0101-OT-AA_foi.pdf

FOI · FOI

A200117_Orig_4_13_1995.pdf

FOI · FOI

ucm054894.pdf

FOI · FOI

ucm061595.pdf

FOI · FOI

ucm069807.pdf

FOI · FOI

N113232_Supp_4_23_1997.pdf

FOI · FOI

N113232-Supp_3_28_1996(2).pdf

FOI · FOI

ucm061758.pdf

FOI · FOI

ucm061589.pdf

FOI · FOI

ucm061587.pdf

FOI · FOI

A200123_Org_2_10_1995.pdf

FOI · FOI

ucm061605.pdf

FOI · FOI

ucm061603.pdf

FOI · FOI

A200154_Orig_05_08_1996.pdf

FOI · FOI

A200068_Orig_07_31_1995.pdf

FOI · FOI

ucm061564.pdf

FOI · FOI

ucm061563.pdf

FOI · FOI

UCM351251.pdf

FOI · FOI

UCM351250.pdf

FOI · FOI

ucm061378.pdf

FOI · FOI

UCM468906.pdf

FOI · FOI

FOI Summary sN 038-439 Approved April 10, 2023.pdf

FOI · FOI

FOI Summary sN 038-439 Approved November 21, 2018.pdf

FOI · FOI

N038439.UCM143044.July 6.2008.pdf

FOI · FOI

ucm049542.pdf

FOI · FOI

ucm061599.pdf

FOI · FOI

A200144_Orig_06_26_1995.pdf

FOI · FOI

ucm117183.pdf

FOI · FOI

N140582_Org_3_15_1988.pdf

FOI · FOI

ucm049522.pdf

FOI · FOI

ucm049521.pdf

FOI · FOI

N008804_Supp_3_14_1996.pdf

FOI · FOI

UCM283519.pdf

FOI · FOI

ucm069857.pdf

FOI · FOI

N130435_Supp_12_10_1993.pdf

FOI · FOI

UCM436419.pdf

FOI · FOI

A200146_Supp_8_15_1996.pdf

FOI · FOI

A200146_Orig_04_22_1994.pdf

FOI · FOI

ucm061679.pdf

FOI · FOI

ucm061678.pdf

FOI · FOI

ucm061676.pdf

FOI · FOI

ucm061380.pdf

FOI · FOI

ucm061580.pdf

FOI · FOI

ucm061578.pdf

FOI · FOI

A200066_Orig_07_15_1994.pdf

FOI · FOI

N038200_Supp_7_10_1993.pdf

FOI · FOI

UCM252253.pdf

FOI · FOI

ucm061570.pdf

FOI · FOI

ucm061566.pdf

FOI · FOI

ucm061565.pdf

FOI · FOI

UCM061648.pdf

FOI · FOI

UCM061645.pdf

FOI · FOI

ucm061757.pdf

FOI · FOI

N140579_Org_12_18_1978.pdf

FOI · FOI summary

N046719_Orig_5_6_1998.pdf

FOI · FOI summary

N046718_Orig_5_6_1998.pdf

FOI · FOI summary

UCM243040.pdf

FOI · FOI summary

ucm118005.pdf

FOI · FOI summary

Veterinary reference (advanced)

Canonical medication sections are above. This legacy block remains available for deeper cross-reference without cluttering the primary workflow.

At a Glance

Quick facts and links to official labeling and safety signals.

Data freshness
  • Storefront facts: Source Roxee | Refreshed May 5, 2026, 10:00 AM UTC
    The storefront fact projection used for browse cards and quick facts.
  • Animal Drugs @ FDA: Source FDA | Refreshed May 5, 2026, 10:00 AM UTC
    Applications/products are imported from FDA export data.
  • Animal Drugs @ FDA previews: Source FDA | Refreshed Mar 13, 2026, 10:01 AM UTC
    Label highlights/doc links are fetched from FDA preview endpoints.
  • Animal Drug Product Listing Directory (NDC): Source FDA | Refreshed May 5, 2026, 10:00 AM UTC
    Package/product NDCs from FDA’s electronic listing directory (XLS).
Official (FDA)
Identity: Generic ingredient • FDA branded products available
Official FDA brands: AGRIMYCIN 200 AX Pharmaceutical Corp Bio-Mycin 200 Liquamycin LA-200 Noromycin 300 LA Oxytet Soluble Oxytetracycline 200 Oxytetracycline Dihydrate Oxytetracycline HCL Oxytetracycline Hydrochloride Pennox 100 Hi-Flo Pennox 343 Pennox 50 TERRA-VET 200 Terra-Vet 200 Terramycin 100 Terramycin 100 MR Terramycin 200 Terramycin 200 Granular Terramycin 50 Terramycin Scours Tetroxy 343 Tetroxy HCA VETRIMYCIN 200 Vetrimycin 200
Manufacturer mapping: Multiple FDA labelers
Catalog species: Both FDA-labeled species: Beef, Beef And Dairy, Beef And Non-Lactating Dairy, Beef and dairy calves, Beef calves, Breeders not laying eggs for human consumption, Breeding, Broilers, Broilers not laying eggs for human consumption, Calves, Calves including preruminating (veal) calves, Cat, Catfish, Cattle, Chicken, Dairy, Dairy calves, Dog, Excluding turkeys producing eggs for human consumption, Fish, Freshwater-Reared Salmonids, Freshwater-reared salmonids weighing up to 55 grams, Growing, Honey Bees, Lobster, No use class stated or implied, Not laying eggs for human consumption, Pacific Salmon, Sheep, Sows, Sows with litters or about to farrow, Swine, Turkey
Rx/OTC: OTC, RX, RX/OTC, VFD
Form/route: Bolus, Capsule, Injectable Solution, Liquid (Solution), Medicated Feed, Powder, Powder for solution, Soluble Powder, Solution, Tablet, Type A Medicated Article Immersion, Intramuscular, Intravenous, Oral, Subcutaneous
Applications: NADA 138-938 • NADA 8622 • NADA 95143 • ANADA 200-537 • ANADA 200-117 • NADA 141-002 • ANADA 200-128 • NADA 113-232 • ANADA 200-306 • ANADA 200-123 • ANADA 200-154 • ANADA 200-068 • ANADA 200-008 • ANADA 200-452 • NADA 95642 • NADA 108-963 • NADA 45143 • NADA 97452 • NADA 47278 • NADA 38439 • ANADA 200-144 • NADA 141-143 • NADA 140-582 • NADA 48287 • NADA 91127 • NADA 99402 • NADA 94114 • NADA 11060 • NADA 8804 • NADA 130-435 • ANADA 200-146 • ANADA 200-247 • ANADA 200-460 • ANADA 200-066 • NADA 38200 • ANADA 200-026 • ANADA 200-232 • NADA 8769 • NADA 11034 • ANADA 200-305 • NADA 94959 • NADA 94960 • NADA 10661 • NADA 103-758 • NADA 7879 • NADA 13470 • NADA 8696
NDC: Packages 0010-4753-01 0010-4753-02 0010-4753-03 13985-035-02 13985-035-04 13985-035-05 Products 0010 13985 23243 43457 46066 51429
Documents: 70 (FOI: 62) • SPL: 74 Label highlights Official documents
Safety (openFDA)
Top reactions: Dog 0 Cat 0 View
Case summaries: 0
openFDA reports are unverified and do not prove causation.

Explore
Linked using: Fda_Label (0.95), Fda_Label (0.95), Fda_Label (0.95)

Diagnosis Codes
ICD10_CM: A27.9
Leptospirosis, unspecified

Counseling and Monitoring Highlights

Global Pet owner/Vet mode is controlled in the header. This section avoids duplicate in-page persona tabs.

Owner-facing counseling points
  • Federal law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption. Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Zero-day slaughter withdrawal in swine. (Contraindication, High)
Top reaction signals
Vomiting (1) Urinary bladder disorder NOS (1) Tiredness (lethargy) (1) Partial deafness (1) Not urinating (1) Nasal discharge (1) Decreased bowel movements (1) Decreased appetite (1)

Identifiers & Packages

Normalized identifiers (NDC/NADA/ANADA) and package metadata from regulator listings.

Identifiers
ANADA: 200008 ANADA: 200026 ANADA: 200066 ANADA: 200068 ANADA: 200096 ANADA: 200117 ANADA: 200123 ANADA: 200128 ANADA: 200144 ANADA: 200146 ANADA: 200154 ANADA: 200232 ANADA: 200247 ANADA: 200305 ANADA: 200306 ANADA: 200452 ANADA: 200460 ANADA: 200537 NADA: 101666 NADA: 103758 NADA: 10661 NADA: 108963 NADA: 11034 NADA: 11060
Package NDC Product NDC Form / Route Status
0010-4753-01 0010 -
0010-4753-02 0010 -
0010-4753-03 0010 -
13985-035-02 13985 -
13985-035-04 13985 -
13985-035-05 13985 -
13985-944-10 13985 -
13985-944-25 13985 -
13985-944-50 13985 -
23243-6759-1 23243 -
23243-6759-2 23243 -
23243-6759-3 23243 -
23243-7430-4 23243 -
23243-7430-5 23243 -
23243-7430-6 23243 -
43457-528-25 43457 -
46066-007-02 46066 -
46066-007-04 46066 -
46066-007-05 46066 -
46066-553-03 46066 -

Enriched Documents

Documents are tiered by source trust: Official, Clinical, Manufacturer, Marketing.

  • Oxytetracycline Dihydrate SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • Oxytetracycline Hydrochloride SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • Oxytetracycline HCL SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • TERRA-VET 200 SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • Terramycin Scours SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • Pennox 343 SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • VETRIMYCIN 200 SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • Bio-Mycin 200 SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • Vetrimycin 200 SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • Liquamycin LA-200 SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • Tetroxy 343 SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • Noromycin 300 LA SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • Oxytetracycline 200 SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • Tetroxy HCA SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • Oxytet Soluble SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • Terra-Vet 200 SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • AGRIMYCIN 200 SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • Terramycin 200 Granular SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • Terramycin 100 SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • Pennox 100 Hi-Flo SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • Pennox 50 SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • Terramycin 50 SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • Terramycin 100 MR SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • Terramycin 200 SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • AX Pharmaceutical Corp SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • Oxytetracycline Hydrochloride SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • N140579_Org_12_18_1978.pdf • FOI summary • Official • April 24, 2026
    FDA FOI summary for application 140579
  • UCM539429.pdf • FOI summary • Official • March 12, 2026
    FDA FOI summary for application 138938
  • UCM523939.pdf • FOI summary • Official • Nov. 12, 2024
    FDA FOI summary for application 8622
  • ucm049517.pdf • FOI summary • Official • Nov. 12, 2024
    FDA FOI summary for application 8622
  • ucm049519.pdf • FOI summary • Official • Nov. 12, 2024
    FDA FOI summary for application 8622
  • FOI Summary sN 008-622 Approved December 30, 2019.pdf • FOI summary • Official • Nov. 12, 2024
    FDA FOI summary for application 8622
  • N046719_Orig_5_6_1998.pdf • FOI summary • Official • Nov. 12, 2024
    FDA FOI summary for application 46719
  • N046718_Orig_5_6_1998.pdf • FOI summary • Official • Nov. 12, 2024
    FDA FOI summary for application 46718
  • N095143_Org_5_30_96.pdf • FOI summary • Official • Aug. 21, 2024
    FDA FOI summary for application 95143
  • ucm079541.pdf • FOI summary • Official • Aug. 21, 2024
    FDA FOI summary for application 95143
  • ucm079545.pdf • FOI summary • Official • Aug. 21, 2024
    FDA FOI summary for application 95143
  • FOI Summary oA 200-537 Approved May 30, 2019.pdf • FOI summary • Official • July 3, 2024
    FDA FOI summary for application 200537
  • A200117_Orig_4_13_1995.pdf • FOI summary • Official • April 30, 2024
    FDA FOI summary for application 200117
  • A-200117-Q-0101-OT-AA_foi.pdf • FOI summary • Official • April 30, 2024
    FDA FOI summary for application 200117

Data Sources & Change Log

Every non-trivial field is expected to include provenance and update timestamps.

Official 112 Clinical 1 Manufacturer 0 Marketing 0
Current Field Facts
  • side_effects: Top reported reactions (openFDA): Anal sac disorder, Behavioural disorder NOS, Corneal ulcer, Hives (see also 'Skin'), Injection site pain, Leucocytosis NOS. (Clinical, 2026-04-11)
  • contraindications: Federal law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used f… (Official, 2026-04-11)
  • contraindications: Federal law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used f… (Official, 2026-02-12)
  • indications: Beef and non-lactating dairy cattle, calves, including pre-ruminating (veal) calves: for the treatment of pneumonia and shipping fever complex associated with … (Official, 2026-05-05)
  • indications: Beef and non-lactating dairy cattle, calves, including pre-ruminating (veal) calves: for the treatment of pneumonia and shipping fever complex associated with … (Official, 2026-05-03)
  • indications: Beef and non-lactating dairy cattle, calves, including pre-ruminating (veal) calves: for the treatment of pneumonia and shipping fever complex associated with … (Official, 2026-05-02)
  • indications: Beef and non-lactating dairy cattle, calves, including pre-ruminating (veal) calves: for the treatment of pneumonia and shipping fever complex associated with … (Official, 2026-04-29)
  • indications: Beef and non-lactating dairy cattle, calves, including pre-ruminating (veal) calves: for the treatment of pneumonia and shipping fever complex associated with … (Official, 2026-04-28)
  • indications: Beef and non-lactating dairy cattle, calves, including pre-ruminating (veal) calves: for the treatment of pneumonia and shipping fever complex associated with … (Official, 2026-04-27)
  • indications: Beef and non-lactating dairy cattle, calves, including pre-ruminating (veal) calves: for the treatment of pneumonia and shipping fever complex associated with … (Official, 2026-04-26)
  • indications: Beef and non-lactating dairy cattle, calves, including pre-ruminating (veal) calves: for the treatment of pneumonia and shipping fever complex associated with … (Official, 2026-04-25)
  • indications: Beef and non-lactating dairy cattle, calves, including pre-ruminating (veal) calves: for the treatment of pneumonia and shipping fever complex associated with … (Official, 2026-04-22)
  • manufacturer_name: Multiple FDA labelers (Official, 2026-05-05)
  • manufacturer_name: Multiple FDA labelers (Official, 2026-05-03)
  • manufacturer_name: Multiple FDA labelers (Official, 2026-05-02)
  • manufacturer_name: Multiple FDA labelers (Official, 2026-04-29)
  • manufacturer_name: Multiple FDA labelers (Official, 2026-04-28)
  • manufacturer_name: Multiple FDA labelers (Official, 2026-04-27)
  • manufacturer_name: Multiple FDA labelers (Official, 2026-04-26)
  • manufacturer_name: Multiple FDA labelers (Official, 2026-04-25)
Recent Revisions
  • side_effects updated 2026-04-11 10:05 by etl_backfill • Backfilled from existing medication fields
  • contraindications updated 2026-04-11 10:05 by etl_backfill • Backfilled from existing medication fields
  • usage updated 2026-04-11 10:05 by etl_backfill • Backfilled from existing medication fields
  • side_effects updated 2026-02-12 22:44 by etl_backfill • Backfilled from existing medication fields
  • contraindications updated 2026-02-12 22:44 by etl_backfill • Backfilled from existing medication fields
  • usage updated 2026-02-12 22:44 by etl_backfill • Backfilled from existing medication fields

FDA Products & Applications (Animal Drugs @ FDA)

Official sponsor/proprietary-name/application-status records linked by active ingredient.

Product Sponsor Application Status Published
Pennox 50® Pennox 100-MR® Pennox 100 Hi-Flo® Pennox 200 Hi-Flo®
VFD
Oxytetracycline
Type A Medicated Article Oral
Pharmgate Inc. NADA 138-938 Approved Mar 12, 2026
TERRAMYCIN-343® TERRAMYCIN® TERRAMYCIN® Soluble Powder Concentrate
RX
Oxytetracycline Hydrochloride
Powder for solution Oral, Immersion
Phibro Animal Health Corp. NADA 8622 Approved Nov 12, 2024
Terramycin® 10 Terramycin® 30 Terramycin® 50 Terramycin® 100 Terramycin® 200 Terramycin® 200 Granular Terramycin® 100MR
VFD
Oxytetracycline
Type A Medicated Article Oral
Phibro Animal Health Corp. NADA 95143 Approved Aug 21, 2024
Tetroxy®-LA
RX
Oxytetracycline
Injectable Solution Intramuscular, Intravenous, Subcutaneous
Bimeda Animal Health Limited ANADA 200-537 Approved Jul 3, 2024
Oxytetracycline Injection
RX
Oxytetracycline
Injectable Solution Intravenous, Intramuscular
Bimeda Animal Health Limited ANADA 200-117 Approved Apr 30, 2024
OXY 500 Calf Bolus OXY 1000 Calf Bolus
OTC
Oxytetracycline Hydrochloride
Bolus Oral
Boehringer Ingelheim Animal Health USA Inc. NADA 141-002 W Aug 25, 2023
AGRIMYCIN® 200
RX
Oxytetracycline Dihydrate
Injectable Solution Intravenous, Subcutaneous, Intramuscular
Huvepharma EOOD ANADA 200-128 Approved Jun 15, 2023
Liquamycin® LA-200®
RX
Oxytetracycline
Injectable Solution Subcutaneous, Intravenous, Intramuscular
Zoetis Inc. NADA 113-232 Approved Jun 15, 2023
Oxytetracycline Injection 200
RX
Oxytetracycline
Injectable Solution Subcutaneous, Intravenous, Intramuscular
Norbrook Laboratories, Ltd. ANADA 200-306 Approved Jun 14, 2023
MAXIM-200
RX
Oxytetracycline
Injectable Solution Subcutaneous, Intravenous, Intramuscular
Huvepharma EOOD ANADA 200-123 Approved Jun 12, 2023
Pennox® 200
RX
Oxytetracycline
Injectable Solution Intravenous, Subcutaneous, Intramuscular
Pharmgate Inc. ANADA 200-154 Approved Jun 7, 2023
MAXIM 100
RX
Oxytetracycline
Injectable Solution Intravenous
Huvepharma EOOD ANADA 200-068 Approved May 26, 2023
Bio-Mycin® 200
RX
Oxytetracycline
Injectable Solution Subcutaneous, Intramuscular, Intravenous
Boehringer Ingelheim Animal Health USA, Inc. ANADA 200-008 Approved May 24, 2023
Oxytet 100
RX
Oxytetracycline
Injectable Solution Intravenous
Norbrook Laboratories, Ltd. ANADA 200-452 Approved May 23, 2023
Oxy-Tet™ Injection Bio-Mycin C
RX/OTC
Oxytetracycline Hydrochloride
Liquid (Solution) Intramuscular
Boehringer Ingelheim Animal Health USA Inc. NADA 95642 W May 3, 2023
Medamycin® 100 MEDAMYCIN®
RX
Oxytetracycline
Injectable Solution Intramuscular
Cronus Pharma Specialities India Private Ltd. NADA 108-963 Approved May 1, 2023
Oxyject®
RX
Oxytetracycline
Injectable Solution Intramuscular
Cronus Pharma Specialities India Private Ltd. NADA 45143 Approved May 1, 2023
OXYJECT® 100 Status™ SQ
RX
Oxytetracycline
Injectable Solution Intramuscular
Cronus Pharma Specialities India Private Ltd. NADA 97452 Approved May 1, 2023
OXY-TET 50™ Bio-Mycin®
RX
Oxytetracycline
Injectable Solution Intramuscular, Intravenous
Cronus Pharma Specialities India Private Ltd. NADA 47278 Approved May 1, 2023
Terramycin® 100 for Fish Terramycin® 200 for Fish
VFD
Oxytetracycline Dihydrate
Type A Medicated Article Oral
Phibro Animal Health Corp. NADA 38439 Approved May 1, 2023
Tetroxy® HCA-280 Tetroxy® HCA-1772 Tetroxy® HCA-1400
RX
Oxytetracycline Hydrochloride
Soluble Powder Oral
Bimeda Animal Health Limited ANADA 200-144 Approved Jan 12, 2023
Noromycin® 300 LA
RX
Oxytetracycline Dihydrate
Solution Intravenous, Subcutaneous, Intramuscular
Norbrook Laboratories, Ltd. NADA 141-143 Approved Nov 18, 2022
Biocyl-50 Biocyl-100
RX
Oxytetracycline Hydrochloride
Injectable Solution Intravenous
Bimeda Animal Health Limited NADA 140-582 Approved Nov 16, 2022
Oxytetracycline-50
RX
Oxytetracycline Hydrochloride
Liquid (Solution) Intramuscular
Huvepharma EOOD NADA 48287 Approved Sep 26, 2022
Rachelle Oxyvet Injection
RX
Oxytetracycline Hydrochloride
Liquid (Solution) Intravenous, Intramuscular
Zoetis Inc. NADA 91127 Approved Sep 26, 2022
Oxyvet-100 Aquachel-100
RX
Oxytetracycline Hydrochloride
Liquid (Solution) Intravenous
Zoetis Inc. NADA 99402 Approved Aug 15, 2022
Terramycin® 100 Liquamycin® 100
RX
Oxytetracycline Hydrochloride
Liquid (Solution) Intramuscular
Zoetis Inc. NADA 94114 Approved Jul 29, 2022
Terramycin® Scours Tablets
RX
Oxytetracycline Hydrochloride
Tablet Oral
Zoetis Inc. NADA 11060 Approved Jul 29, 2022
TM-50® TM-50® D TM-100® TM-100®D
VFD
Oxytetracycline Hydrochloride
Type A Medicated Article Oral
Phibro Animal Health Corp. NADA 8804 Approved Jul 13, 2021
Oxytet® Soluble OXYMarine™
RX
Oxytetracycline Hydrochloride
Soluble Powder Immersion
Huvepharma EOOD NADA 130-435 Approved Jun 12, 2019
Tetroxy® 25
RX
Oxytetracycline Hydrochloride
Soluble Powder Oral
Bimeda Animal Health Limited ANADA 200-146 Approved Mar 17, 2019
Tetroxy® 343
RX
Oxytetracycline Hydrochloride
Powder Oral, Immersion
Bimeda Animal Health Limited ANADA 200-247 Approved Mar 17, 2019
Tetroxy® Aquatic
RX
Oxytetracycline Hydrochloride
Liquid (Solution) Immersion
Bimeda Animal Health Limited ANADA 200-460 Approved Oct 2, 2018
AGRIMYCIN®-343
RX
Oxytetracycline Hydrochloride
Soluble Powder Oral
Huvepharma EOOD ANADA 200-066 Approved Jul 2, 2018
OXY WS™
RX
Oxytetracycline Hydrochloride
Soluble Powder Oral
Phibro Animal Health Corp. NADA 38200 Approved May 15, 2017
Pennox 343®
RX
Oxytetracycline Hydrochloride
Soluble Powder Immersion, Oral
Pharmgate Inc. ANADA 200-026 Approved Jan 3, 2017
Geomycin 200
OTC
Oxytetracycline
Liquid (Solution) Subcutaneous, Intramuscular, Intravenous
Pliva, d. d. ANADA 200-232 W Jun 1, 2016
Liquamycin® Injectable Terramycin® Injectable
RX
Oxytetracycline Hydrochloride
Liquid (Solution) Intravenous, Intramuscular, Subcutaneous
Zoetis Inc. NADA 8769 Approved Jun 1, 2016
Liquimast Solution for Mastitis
OTC
Oxytetracycline Hydrochloride
Pfizer, Inc. NADA 11034 W Jun 1, 2016
Oxytetracycline Hydrochloride Soluble Powder
OTC
Oxytetracycline Hydrochloride
Liquid (Solution) Oral
Vetoquinol N.-A., Inc. ANADA 200-305 W Jun 1, 2016
Oxytetracycline Premix
OTC
Oxytetracycline Hydrochloride
Purina Mills, Inc. NADA 94959 W Jun 1, 2016
Purina® Mix-R-Mycin Concentrate
OTC
Oxytetracycline Hydrochloride
Purina Mills, Inc. NADA 94960 W Jun 1, 2016
Terramycin® Egg Formula
OTC
Oxytetracycline Hydrochloride
Pfizer, Inc. NADA 10661 W Jun 1, 2016
Terramycin® Premix
OTC
Oxytetracycline Hydrochloride
Medicated Feed Oral
Pfizer, Inc. NADA 103-758 W Jun 1, 2016
Terramycin® Vet Capsules
RX
Oxytetracycline Hydrochloride
Capsule Oral
Zoetis Inc. NADA 7879 Approved Jun 1, 2016
TM®-10 Premix
OTC
Oxytetracycline Hydrochloride
Pfizer, Inc. NADA 13470 W Jun 1, 2016
TM®-5 Antibiotic Feed Supplement
OTC
Oxytetracycline (Monoalkyl Trimethyl Ammonium Salt)
Pfizer, Inc. NADA 8696 W Jun 1, 2016

Data source: FDA Animal Drugs @ FDA (public search export).

What It's For (FDA Label Highlights)

Extracted from FDA Animal Drugs @ FDA product labeling. Always confirm details with your veterinarian.

Species: Honey Bees • Breeding • No use class stated or implied • Growing, Over 400 Pounds • Beef • Calves • Dairy, non-lactating • Broilers • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Sheep, No Use Class Stated Or Implied
Composition / specifications
Type A medicated articles contain 50 grams oxytetracycline per pound.
Chickens
Indication

For control of infectious synovitis caused by Mycoplasma synoviae; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

100 to 200 grams per ton of feed. Feed continuously for 7-14 days.

Limitations
Indication

For control of chronic respiratory disease (CRD) and air sac infection caused by M. gallisepticum and Escherichia coli susceptible to oxytetracycline.

Dosage

400 grams per ton of feed. Feed continuously for 7-14 days.

Limitations
Broiler chickens
Indication

For reduction of mortality due to air sacculitis (air-sac-infection) caused by E. coli susceptible to oxytetracycline.

Dosage

500 grams per ton of feed. Feed continuously for 5 days.

Limitations
Turkeys
Indication

For control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.

Dosage

100 grams per ton of feed. Feed continuously for 7 to 14 days.

Limitations
Indication

For control of infectious synovitis caused by M. synoviae susceptible to oxytetracycline.

Dosage

200 grams per ton of feed. Feed continuously for 7 to 14 days.

Limitations
Indication

For control of complicating bacterial organisms associated with bluecomb (transmissible enteritis; coronaviral enteritis) susceptible to oxytetracycline.

Dosage

25 milligrams per pound body weight. Feed continuously for 7 to 14 days.

Limitations
Swine
Indication

For treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis susceptible to oxytetracycline and treatment of bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound body weight daily in feed. Feed continuously for 7 to 14 days.

Limitations
Swine (breeding)
Indication

For control and treatment of leptospirosis (reducing the incidence of abortion and shedding of leptospirae) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage

10 milligrams per pound body weight daily in feed. Feed continuously for 7 to 14 days.

Limitations
Cattle (calves, beef, nonlactating dairy)
Indication

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia (shipping fever complex) caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound body weight daily in feed. Feed continuously for 7 to 14 days.

Limitations
Cattle
Indication

For prevention and treatment of the early stages of shipping fever complex.

Dosage

0.5 to 2.0 grams per head per day in feed. Feed 3 to 5 days before and after arrival in feedlots.

Limitations
Cattle (growing, over 400 pounds body weight)
Indication

For reduction of the incidence of liver abscesses.

Dosage

75 milligrams per head per day in feed.

Limitations
Sheep
Indication

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily in feed. Feed continuously for 7 to 14 days.

Limitations
Honey bees
Indication

For control of American Foulbrood caused by Paenibacillus larvae, and European Foulbrood caused by Streptococcus pluton susceptible to oxytetracycline.

Dosage

200 milligrams / oz dusting of Type C medicated feed per colony every 4 to 5 days for a total of 3 applications

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: Honey Bees • Fish, Finfish, Fry And Fingerlings • Breeding • No use class stated or implied • Beef • Calves • Dairy, females Under 20 months of age • Growing • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Sheep, No Use Class Stated Or Implied
Composition / specifications
Each 1.32 grams of TERRAMYCIN-343® powder contains 1 gram of OTC HCl (packets: 2.39, 4.78, and 9.55 oz.; jars: 2.25 lbs.; and pails: 4.5 lbs.).
Chickens
Indication
Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.
Dosage
200 to 400 milligrams per gallon of drinking water.
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.
Indication

Control of chronic respiratory disease (CRD) and air sac infection caused by Mycoplasma gallisepticum and E. coli susceptible to oxytetracycline; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage
400 to 800 milligrams per gallon of drinking water.
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.
Turkeys
Indication
Control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.
Dosage
200 - 400 milligrams per gallon of drinking water.
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.
Indication
Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.
Dosage
400 milligrams per gallon of drinking water.
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.
Turkeys (Growing)
Indication
Control of complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis) susceptible to oxytetracycline.
Dosage
25 milligrams per pound of body weight daily
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.
Swine
Indication

Control and treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight
Limitations

Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Zero-day slaughter withdrawal in swine.

Breeding Swine
Indication
Control and treatment of leptospirosis (reducing the incidence of abortions and shedding of leptospira) caused by Leptospira Pomona susceptible to oxytetracycline.
Dosage
10 milligrams per pound of body weight
Limitations

Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Zero–day slaughter withdrawal in swine.

Cattle (calves, beef, and non lactating dairy)
Indication

Control and treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight
Limitations
Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as sole source of oxytetracycline. Do not administer this product with milk or milk replacers. Administer 1 hour before or 2 hours after feeding milk or milk replacers. Withdraw 5 days prior to slaughter. A milk discard period has not been established for this product in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older.
Sheep
Indication

Control and treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight
Limitations

Prepare a fresh solution daily. Administer up to 14 days.Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Withdraw 5 days before slaughter.

Honey Bees
Indication

Control and treatment of American foul brood caused by Paenibacillus larvae.

Dosage
200 milligrams per colony, administered via either a 1:1 sugar syrup (equal parts of sugar and water weight to weight) or dusting with a powdered sugar mixture.
Limitations

The drug is administered in 3 applications of sugar syrup or 3 dustings at 4- to 5- day intervals. The drug should be fed early in the spring or fall and consumed by the bees before main honey flow begins to avoid contamination of production honey. Remove at least 6 weeks prior to main honey flow. Dusting of uncapped brood cells has been reported to cause death of larval honey bees. Do not dust uncapped brood cells.

Finfish
Indication
For skeletal marking of finfish fry and fingerlings.
Dosage
Immerse fish in a solution containing 200 to 700 mg oxytetracycline hydrochloride (buffered) per liter of water for 2 to 6 hours.
Limitations
Solution should be tested on a small number of fish before full-scale use. Do not discharge marking immersion water containing oxytetracycline into surface waters. Oxytetracycline HCl will acidify the water. The pH should be maintained at an acceptable level for fish by the addition of a buffer. Monitor water quality and temperature.

FDA page: Open in Animal Drugs @ FDA

Species: Honey Bees • Breeding • No use class stated or implied • Beef • Calves • Dairy, non-lactating • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Sheep, No Use Class Stated Or Implied
Composition / specifications
Type A medicated articles contain 10 grams oxytetracycline per pound.
Chickens
Indication

For control of infectious synovitis caused by Mycoplasma synoviae; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

100 to 200 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. At 500 g/ton level,withdraw 24 hours before slaughter. Zero-day withdrawal period for lower use levels. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues. Do not administer to chickens producing eggs for human consumption.

Indication

For control of chronic respiratory disease (CRD) and air sac infection caused by Mycoplasma gallisepticum and Escherichia coli susceptible to oxytetracycline.

Dosage

400 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. At 500 g/ton level, withdraw 24 hours before slaughter. Zero-day withdrawal period for lower use levels. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues. Do not administer to chickens producing eggs for human consumption.

Indication

For reduction of mortality due to air sacculitis (air-sac-infection) caused by Escherichia coli susceptible to oxytetracycline.

Dosage

500 grams per ton of feed.

Limitations

Feed continuously for 5 days. At 500 g/ton level, withdraw 24 hours before slaughter. Zero-day withdrawal period for lower use levels. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues. Do not administer to chickens producing eggs for human consumption.

Turkeys
Indication

For control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.

Dosage

100 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. Do not administer to turkeys producing eggs for human consumption.

Indication

For control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage

200 grams per ton of feed.

Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not administer to turkeys producing eggs for human consumption.

Indication

For control of complicating bacterial organisms associated with bluecomb (transmissible enteritis; coronaviral enteritis) susceptible to oxytetracycline.

Dosage

25 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not administer to turkeys producing eggs for human consumption.

Swine
Indication

For treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis susceptible to oxytetracycline and treatment of bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days.

Swine (breeding)
Indication

For control and treatment of leptospirosis (reducing the incidence of abortion and shedding of leptospirae) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 14 days.

Cattle (calves, beef, and nonlactating dairy)
Indication

For growing cattle (over 400 lb) for the reduction of the incidence of liver abscesses.

Dosage

75 milligrams per head per day.

Limitations

Feed continuously.

Indication

For prevention and treatment of the early stages of shipping fever complex.

Dosage

0.5 to 2.0 grams per head per day.

Limitations

Feed 3 to 5 days before and after arrival in feedlots.

Indication

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia (shipping fever complex) caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Zero-day withdrawal time.

Cattle (calves)
Indication

For treatment of bacterial enteritis caused by Escherichia coli susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days in milk replacer or starter feed. Zero-day withdrawal time.

Sheep
Indication

For treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Withdrawal 5 days before slaughter.

Honey bees
Indication

For control of American Foulbrood caused by Paenibacillus larvae, and European Foulbrood caused by Streptococcus pluton susceptible to oxytetracycline.

Dosage

200 milligrams per colony.

Limitations

Remove at least 6 weeks prior to main honey flow.

FDA page: Open in Animal Drugs @ FDA

Species: No use class stated or implied • Beef And Dairy • Calves including preruminating (veal) calves
Composition / specifications
200 mg/mL of oxytetracycline base as oxytetracycline dihydrate
Cattle (beef, dairy, and calves including preruminating (veal) calves)
Indication

For the treatment of the following conditions : 1) bacterial pneumonia caused by Pasteurella spp. (shipping fever) in calves and yearlings, where retreatment is impractical due to husbandry conditions, such as cattle on range, or where repeated restraint is inadvisable; 2) infectious bovine keratoconjunctivitis (pinkeye) cause by Moraxella bovis.

Dosage

A single dosage of 9 milligrams per pound of body weight administered by subcutaneous injection.

Limitations
Indication

For the treatment of pneumonia and shipping fever complex associated with Pasteurella spp. and Haemophilus spp.; infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis; foot rot and diphtheria caused by Fusobacterium necrophorum; bacterial enteritis (scours) caused by Escherichia coli; wooden tongue caused by Actinobacillus lignieresii; leptospirosis caused by Leptospira pomona; and wound infections and acute metritis caused by strains of staphylococci and streptococci organisms sensitive to oxytetracycline.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day, administered by subcutaneous or intravenous injection. In the treatment of severe foot rot and advanced cases of other indicated diseases, a dosage level of 5 milligrams per pound of body weight per day is recommended. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Limitations
Swine
Indication

For the treatment of bacterial pneumonia caused by Pasteurella multocida, where retreatment is impractical due to husbandry conditions or where repeated restraint is inadvisable.

Dosage

A single dosage of 9 milligrams of per pound of body weight administered intramuscularly.

Limitations
Indication

For the treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli; pneumonia caused by Pasteurella multocida; and leptospirosis caused by Leptospira pomona.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day administered by intramuscular injection.
Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Limitations
Sows
Indication

As an aid in the control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.

Dosage

3 mg of oxytetracycline per lb of body weight administered once by intramuscular injection approximately 8 hours before farrowing or immediately after completion of farrowing.

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: No use class stated or implied • Sows • Beef • Dairy, non-lactating
Composition / specifications
200 milligrams oxytetracycline per mL
Sows
Indication

As an aid in the control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli

Dosage

3 mg of oxytetracycline per lb of body weight administered once by intramuscular injection approximately 8 hours before farrowing or immediately after completion of farrowing.

Limitations
Cattle (beef and nonlactating dairy)
Indication

For the treatment of the following conditions : 1) bacterial pneumonia caused by Pasteurella spp. (shipping fever) in yearlings, where re-treatment is impractical due to husbandry conditions, such as cattle on range, or where repeated restraint is inadvisable; 2) infectious bovine keratoconjunctivitis (pinkeye) cause by Moraxella bovis.

Dosage

A single dosage of 9 milligrams per pound of body weight administered intramuscularly. 

Limitations
Indication

For the treatment of pneumonia and shipping fever complex associated with Pasteurella spp. and Hemophilus spp.; infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis; foot rot and diphtheria caused by Fusobacterium necrophorum; bacterial enteritis (scours) caused by Escherichia coli; wooden tongue caused by Actinobacillus lignieresii; leptospirosis caused by Leptospira pomona; and wound infections and acute metritis caused by strains of staphylococci and streptococci organisms sensitive to oxytetracycline.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day, administered by intravenous or intramuscular injection. In the treatment of severe foot rot and advanced cases of other indicated diseases, a dosage level of 5 milligrams per pound of body weight per day is recommended. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Limitations
Swine
Indication

For the treatment of bacterial pneumonia caused by Pasteurella multocida, where re-treatment is impractical due to husbandry conditions or where repeated restraint is inadvisable.

Dosage

A single dosage of 9 milligrams of per pound of body weight administered intramuscularly.

Limitations
Indication

For the treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli; pneumonia caused by Pasteurella multocida; and leptospirosis caused by Leptospira pomona.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day administered by intramuscular injection. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: Beef • Dairy, non-lactating
Composition / specifications
Each bolus contains 500 or 1000 milligrams of oxytetracycline hydrochloride.
Beef and Dairy Calves
Indication
For control of bacterial enteritis caused by Salmonella typhimurium and Escherichia coli (colibacillosis) and bacterial pneumonia (shipping fever complex, pasteurellosis) caused by Pasteurella multocida.
Dosage
250 milligrams per 100 pounds of body weight every 12 hours (5 milligrams per pound of body weight daily in two doses) for up to four consecutive days.
Limitations
Dosage should continue until the animal returns to normal and for 24 hours to 48 hours after symptoms have subsided. Treatment should not exceed 4 consecutive days. Do not exceed 500 milligrams per 100 pounds of body weight every 12 hours (10 milligrams per pound daily). Discontinue treatment 7 days prior to slaughter. Not for use in lactating dairy cattle. A withdrawal period has not been established for this product in pre-ruminating calves. Do not use in calves to be processed for veal.
Indication
For treatment of bacterial enteritis caused by Salmonella typhimurium and Escherichia coli (colibacillosis) and bacterial pneumonia (shipping fever complex, pasteurellosis) caused by Pasteurella multocida.
Dosage
500 milligrams per 100 pound of body weight every 12 hours (10 milligrams per pound of body weight daily in two doses).
Limitations
Dosage should continue until the animal returns to normal and for 24 hours to 48 hours after symptoms have subsided. Treatment should not exceed 4 consecutive days. Do not exceed 500 milligrams per 100 pounds of body weight every 12 hours (10 milligrams per pound daily). Discontinue treatment 7 days prior to slaughter. Not for use in lactating dairy cattle. A withdrawal period has not been established for this product in pre-ruminating calves. Do not use in calves to be processed for veal.

FDA page: Open in Animal Drugs @ FDA

Species: No use class stated or implied • Sows • Beef And Dairy • Calves including preruminating (veal) calves
Composition / specifications
200 mg oxytetracycline per mL
Beef cattle, dairy cattle, and calves including prerumenative (veal) calves
Indication

For the treatment of the following conditions: 1) bacterial pneumonia caused by Pasteurella spp. (shipping fever) in calves and yearlings, where retreatment is impractical due to husbandry conditions, such as cattle on range, or where repeated restraint is inadvisable; 2) infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis.

Dosage

A single dosage of 9 milligrams oxytetracycline per pound of body weight administered subcutaneously.


Limitations
Indication

For the treatment of pneumonia and shipping fever complex associated with Pasteurella spp. and Haemophilus spp.; infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis; foot rot and diphtheria caused by Fusobacterium necrophorum; bacterial enteritis (scours) caused by Escherichia coli; wooden tongue caused by Actinobacillus lignieresii; leptospirosis caused by Leptospira pomona; and wound infections and acute metritis caused by strains of staphylococci and streptococci organisms sensitive to oxytetracycline.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day, administered by subcutaneous or intravenous injection. In the treatment of severe foot rot and advanced cases of other indicated diseases, a dosage of 5 milligrams per pound of body weight per day is recommended. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Limitations
Swine
Indication

For the treatment of bacterial pneumonia caused by Pasteurella multocida, where retreatment is impractical due to husbandry conditions or where repeated restraint is inadvisable.

Dosage

A single dosage of 9 milligrams oxytetracycline per pound of body weight administered intramuscularly.


Limitations
Indication

For the treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli; pneumonia caused by Pasteurella multocida; and leptospirosis caused by Leptospira pomona.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day administered by intramuscular injection. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Limitations
Swine (sows)
Indication

As an aid in the control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.

Dosage

3 mg of oxytetracycline per lb of body weight administered once by intramuscular injection approximately 8 hours before farrowing or immediately after completion of farrowing.

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: No use class stated or implied • Sows • Calves, Including Prerumenative Veal • Beef • Dairy
Composition / specifications
200 mg oxytetracycline base as oxytetracycline dihydrate per mL
Beef cattle, dairy cattle, and calves including prerumenative (veal) calves
Indication

Treatment of infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis; and in the treatment of the following conditions where retreatment is impractical due to husbandry conditions, such as cattle on range, or where their repeated restraint is inadvisable: bacterial pneumonia caused by Pasteurella spp. (shipping fever) in calves and yearlings, and anaplasmosis caused by Anaplasma marginale.

Dosage

A single dosage of 9 milligrams oxytetracycline per pound of body weight administered intramuscularly or subcutaneously.

Limitations
Indication

For the treatment of pneumonia and shipping fever complex associated with Pasteurella spp. and Hemophilus spp.; infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis; foot rot and diphtheria caused by Fusobacterium necrophorum; bacterial enteritis (scours) caused by Escherichia coli; wooden tongue caused by Actinobacillus lignieresii; leptospirosis caused by Leptospira pomona; anaplasmosis caused by Anaplasma marginale; anthrax caused by Bacillus anthracis; and wound infections and acute metritis caused by strains of staphylococci and streptococci organisms sensitive to oxytetracycline.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day, administered by intravenous, subcutaneous, or intramuscular injection. In the treatment of severe foot-rot and advanced cases of other indicated diseases, a dosage of 5 milligrams per pound of body weight per day is recommended. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Limitations
Swine
Indication

For the treatment of bacterial pneumonia caused by Pasteurella multocida, where retreatment is impractical due to husbandry conditions or where repeated restraint is inadvisable.

Dosage

A single dosage of 9 milligrams of oxytetracycline per pound of body weight administered intramuscularly.

Limitations
Indication

For the treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli; pneumonia caused by Pasteurella multocida; and leptospirosis caused by Leptospira pomona.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day administered by intramuscular injection. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Limitations
Swine (sows)
Indication

As an aid in the control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.

Dosage

3 mg of oxytetracycline per lb of body weight administered once by intramuscular injection approximately 8 hours before farrowing or immediately after completion of farrowing.

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: No use class stated or implied • Sows • Beef • Dairy
Composition / specifications
200 mg oxytetracycline per mL
Beef cattle; dairy cattle; and calves, including preruminating (veal) calves
Indication

For the treatment of the following conditions: 1) bacterial pneumonia caused by Pasteurella spp. (shipping fever) in calves and yearlings, where retreatment is impractical due to husbandry conditions, such as cattle on range, or where repeated restraint is inadvisable; 2) infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis.

Dosage

A single dosage of 9 milligrams oxytetracycline per pound of body weight administered intramuscularly or subcutaneously.

Limitations
Indication

For the treatment of pneumonia and shipping fever complex associated with Pasteurella spp. and Haemophilus spp; infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis; foot rot and diphtheria caused by Fusobacterium necrophorum; bacterial enteritis (scours) caused by Escherichia coli; wooden tongue caused by Actinobacillus lignieresii; leptospirosis caused by Leptospira pomona; and wound infections and acute metritis caused by strains of staphylococci and streptococci organisms sensitive to oxytetracycline.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day, administered by intravenous, subcutaneous, or intramuscular injection. In the treatment of severe foot-rot and advanced cases of other indicated diseases, a dosage of 5 milligrams per pound of body weight per day is recommended. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Limitations
Swine
Indication

 For the treatment of bacterial pneumonia caused by Pasteurella multocida, where re-treatment is impractical due to husbandry conditions or where repeated restraint is inadvisable.

Dosage

A single dosage of 9 milligrams of oxytetracycline per pound of body weight administered intramuscularly.

Limitations
Indication

For the treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli; pneumonia caused by Pasteurella multocida; and leptospirosis caused by Leptospira pomona.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day administered by intramuscular injection. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Limitations
Swine (sows)
Indication

As an aid in the control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.

Dosage

3 mg of oxytetracycline per lb of body weight administered once by intramuscular injection approximately 8 hours before farrowing or immediately after completion of farrowing.

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: No use class stated or implied • Sows with litters or about to farrow • Calves, Including Prerumenative Veal • Beef • Dairy
Composition / specifications
200 milligrams oxytetracycline per mL.
Cattle (beef cattle; dairy cattle; calves, including preruminating (veal) calves)
Indication

For the treatment of the following conditions: 1) bacterial pneumonia caused by Pasteurella spp. (shipping fever) in calves and yearlings, where retreatment is impractical due to husbandry conditions, such as cattle on range, or where repeated restraint is inadvisable; 2) infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis.

Dosage

A single dosage of 9 milligrams oxytetracycline per pound of body weight administered intramuscularly or subcutaneously.

Limitations
Indication

For the treatment of pneumonia and shipping fever complex associated with Pasteurella spp. and Hemophilus spp; infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis; foot-rot and diphtheria caused by Fusobacterium necrophorum; bacterial bacterial enteritis (scours) caused by Escherichia coli; wooden tongue caused by Actinobacillus lignieresii; leptospirosis caused by Leptospira pomona; and wound infections and acute metritis caused by strains of staphylococci and streptococci organisms sensitive to oxytetracycline.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day, administered by intravenous, subcutaneous, or intramuscular injection. In the treatment of severe foot-rot and advanced cases of other indicated diseases, a dosage of 5 milligrams per pound of body weight per day is recommended. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Limitations
Swine
Indication

Where re-treatment for pneumonia is impractical. For the treatment of bacterial pneumonia caused by Pasteurella multocida, where re-treatment is impractical due to husbandry conditions or where repeated restraint is inadvisable.

Dosage

A single dosage of 9 milligrams oxytetracycline per pound of body weight administered intramuscularly.

Limitations
Indication

For the treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli; pneumonia caused by Pasteurella multocida; and leptospirosis caused by Leptospira pomona.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day administered by intramuscular injection. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Limitations
Sows
Indication

As an aid in the control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.

Dosage

3 mg of oxytetracycline per lb of body weight administered once by intramuscular injection approximately 8 hours before farrowing or immediately after completion of farrowing.

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: No use class stated or implied • Sows with litters or about to farrow • Beef • Dairy • Calves including preruminating (veal) calves
Composition / specifications
Each mL contains 200 mg of oxytetracycline base as amphoteric oxytetracycline
Cattle (beef cattle; dairy cattle; calves, including preruminating (veal) calves)
Indication

For the treatment of the following conditions: 1) bacterial pneumonia caused by Pasteurella spp. (shipping fever) in calves and yearlings, where retreatment is impractical due to husbandry conditions, such as cattle on range, or where repeated restraint is inadvisable; 2) infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis.

Dosage

A single dosage of 9 milligrams oxytetracycline per pound of body weight administered subcutaneously.

Limitations
Indication

For the treatment of pneumonia and shipping fever complex associated with Pasteurella spp. and Hemophilus spp.; infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis; foot rot and diphtheria caused by Fusobacterium necrophorum; bacterial enteritis (scours) caused by Escherichia coli; wooden tongue caused by Actinobacillus lignieresii; leptospirosis caused by Leptospira pomona; and wound infections and acute metritis caused by strains of staphylococci and streptococci organisms sensitive to oxytetracycline.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day, administered by subcutaneous or intravenous injection. In the treatment of severe foot rot and advanced cases of other indicated diseases, a dosage of 5 milligrams per pound of body weight per day is recommended. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Limitations
Swine
Indication

For the treatment of bacterial pneumonia caused by Pasteurella multocida, where retreatment is impractical due to husbandry conditions or where repeated restraint is inadvisable.

Dosage

A single dosage of 9 milligrams oxytetracycline per pound of body weight administered intramuscularly.

Limitations
Indication

For the treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli; pneumonia caused by Pasteurella multocida; and leptospirosis caused by Leptospira pomona.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day administered by intramuscular injection. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Limitations
Sows
Indication

As an aid in the control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.

Dosage

3 mg of oxytetracycline per lb of body weight administered once by intramuscular injection approximately 8 hours before farrowing or immediately after completion of farrowing.

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: Beef • Dairy, non-lactating • Beef and dairy calves, excluding veal calves
Composition / specifications
Each milliliter of sterile solution contains 100 milligrams of oxytetracycline hydrochloride.
Cattle (beef, non-lactating dairy, and beef and dairy calves [excluding veal])
Indication

Treatment of bacterial pneumonia and shipping fever complex associated with Pasteurella spp.; bacterial enteritis (scours) caused by Escherichia coli; necrotic pododermatitis (foot rot) and calf diphtheria caused by Fusobacterium necrophorum; wooden tongue caused by Actinobacillus lignieresi; and wound infections, acute metritis, and traumatic injury caused by oxytetracycline susceptible staphylococcal and streptococcal organisms.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day (3 to 5 mL per 100 pounds of body weight) by intravenous injection. Severe foot rot and the severe forms of the indicated diseases should be treated with 5 mg per pound of body weight. Treatment should be continued 24 to 48 hours following remission of disease symptoms, not to exceed a total of 4 consecutive days.

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: No use class stated or implied • Sows with litters or about to farrow • Beef • Dairy
Composition / specifications
200 milligrams oxytetracycline per milliliter.
Sows
Indication

As an aid in the control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.

Dosage

3 mg of oxytetracycline per lb of body weight administered once by intramuscular injection approximately 8 hours before farrowing or immediately after completion of farrowing.

Limitations
Cattle (beef and dairy)
Indication

For the treatment of the following conditions : 1) bacterial pneumonia caused by Pasteurella spp. (shipping fever) in yearlings, where re-treatment is impractical due to husbandry conditions, such as cattle on range, or where repeated restraint is inadvisable; 2) infectious bovine keratoconjunctivitis (pinkeye) cause by Moraxella bovis.

Dosage

A single dosage of 9 milligrams per pound of body weight administered intramuscularly or subcutaneously.
Intramuscular administration is not recommended according to Beef Quality Assurance Guidelines.

Limitations
Indication

For the treatment of pneumonia and shipping fever complex associated with Pasteurella spp. and Haemophilus spp.; infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis; foot-rot and diphtheria caused by Fusobacterium necrophorum; bacterial enteritis (scours) caused by Escherichia coli; wooden tongue caused by Actinobacillus lignieresii; leptospirosis caused by Leptospira pomona; and wound infections and acute metritis caused by strains of staphylococci and streptococci organisms sensitive to oxytetracycline.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day, administered by intravenous, subcutaneous, or intramuscular injection. In the treatment of severe foot rot and advanced cases of other indicated diseases, a dosage level of 5 milligrams per pound of body weight per day is recommended. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment. Intramuscular administration is not recommended according to Beef Quality Assurance Guidelines.

Limitations
Swine
Indication

For the treatment of bacterial pneumonia caused by Pasteurella multocida, where re-treatment is impractical due to husbandry conditions or where repeated restraint is inadvisable.

Dosage

A single dosage of 9 milligrams of per pound of body weight administered intramuscularly.

Limitations
Indication

For the treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli; pneumonia caused by Pasteurella multocida; and leptospirosis caused by Leptospira pomona.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day administered by intramuscular injection. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days. Consult your veterinarian if improvement is not noted within 24 to 48 hours of the beginning of treatment.

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: Beef And Non-Lactating Dairy • Beef and dairy calves, excluding veal calves
Composition / specifications
Each milliliter of sterile solution contains 100 milligrams of oxytetracycline hydrochloride.
Cattle (beef, nonlactating dairy, and beef and dairy calves [excluding veal])
Indication

Treatment of bacterial pneumonia and shipping fever complex associated with Pasteurella spp.; bacterial enteritis (scours) caused by Escherichia coli; necrotic pododermatitis (foot rot) and calf diphtheria caused by Fusobacterium necrophorum; wooden tongue caused by Actinobacillus lignieresi; and wound infections, metritis, and traumatic injury caused by oxytetracycline susceptible staphylococcal and streptococcal organisms.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day (3 to 5 mL per 100 pounds of body weight)
by intravenous injection. Severe foot rot and the severe forms of the indicated diseases should be treated with 5 mg per pound of body weight. Treatment should be continued 24 to 48 hours following remission of disease symptoms, not to exceed a total of 4 consecutive days.

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: No use class stated or implied • Sows with litters or about to farrow • Beef • Calves • Dairy, non-lactating
Composition / specifications
Each milliliter of sterile solution contains 100 milligrams of oxytetracycline (as oxytetracycline hydrochloride).
Swine
Indication

For treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli, pneumonia caused by Pasteurella multocida, and leptospirosis caused by Leptospira pomona.

Dosage
Three to 5 milligrams of oxytetracycline per pound of body weight per day. Administer intramuscularly.
Limitations
Do not inject more than 5 milliliters per site. Do not use for more than 4 consecutive days. Discontinue treatment at least 26 days before slaughter.
Swine (sows)
Indication

As an aid in control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.

Dosage
3 milligrams of oxytetracycline per pound of body weight, approximately 8 hours before farrowing or immediately after completion of farrowing. Administer intramuscularly.
Limitations
Do not inject more than 5 milliliters per site. Do not use for more than 4 consecutive days. Discontinue treatment at least 26 days before slaughter.
Cattle (beef and nonlactating dairy)
Indication

Treatment of diseases due to oxytetracycline-susceptible organisms as follows: Pneumonia and shipping fever complex associated with Pasteurella species, Hemophilus species, and Klebsiella species, foot-rot and diphtheria caused by Spherophorus necrophorus, bacterial enteritis (scours) caused by Escherichia coli, wooden tongue caused by Actinobacillus lignieresi, leptospirosis caused by Leptospira pomona, and wound infections and acute metritis caused by Staphylococcus species and Streptococcus species. If labeled for use by or on the order of a licensed veterinarian, it may be used for the treatment of anaplasmosis caused by Anaplasma marginale.

Dosage
Three to 5 milligrams of oxytetracycline per pound of body weight per day; 5 milligrams per pound of body weight per day for the treatment of anaplasmosis, severe foot-rot, and severe cases of other indicated diseases. For 100-milligram-per-milliliter solution, administer intramuscularly.
Limitations
Treatment of all diseases should be instituted early and continue for 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 4 consecutive days. Consult your veterinarian if no improvement is noted within 48 hours. Do not inject more than 10 milliliters per site in adult cattle, reducing the volume according to age and body size to 0.5 to 2 milliliters in small calves. Exceeding the highest recommended dose of 5 milligrams per pound of body weight, administering at recommended levels for more than 4 consecutive days, and/or exceeding 10 milliliters intramuscularly per injection site may result in antibiotic residues beyond the withdrawal time. Discontinue treatment at least 18 days prior to slaughter. Not for use in lactating dairy cattle. This drug product is not approved for use in female dairy cattle 20 months of age or older, including dry dairy cows. Use in these cattle may cause drug residues in milk and /or in calves born to these cows.

FDA page: Open in Animal Drugs @ FDA

Species: Beef And Non-Lactating Dairy • Beef and dairy calves, excluding veal calves
Composition / specifications
Each milliliter of sterile solution contains 100 milligrams of oxytetracycline hydrochloride.
Cattle (beef, nonlactating dairy, and beef and dairy calves [excluding veal])
Indication

Treatment of bacterial pneumonia and shipping fever complex associated with Pasteurella spp.; bacterial enteritis (scours) caused by Escherichia coli; necrotic pododermatitis (foot rot) and calf diphtheria caused by Fusobacterium necrophorum; wooden tongue caused by Actinobacillus lignieresi; and wound infections, acute metritis, and traumatic injury caused by oxytetracycline-susceptible staphylococcal and streptococcal organisms.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day (3 to 5 mL per 100 pounds of body weight) by intravenous injection. Severe foot rot and the severe forms of the indicated diseases should be treated with 5 mg per pound of body weight. Treatment should be continued 24 to 48 hours following remission of disease symptoms, not to exceed a total of 4 consecutive days.

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: Beef And Non-Lactating Dairy • Beef calves • Dairy calves
Composition / specifications
The drug contains 50 milligrams of oxytetracycline hydrochloride in each milliliter of sterile solution.
Cattle (beef and non-lactating dairy, beef and dairy calves)
Indication

Treatment of pneumonia and shipping fever complex associated with Pasteurella sp., Hemophilus sp., and Klebsiella sp., bacterial enteritis (scours) caused by Escherichia coli, foot rot and diphtheria caused by Spherophorus necrophorus, wooden tongue caused by Actinobacillus lignieresi, leptospirosis caused by Leptospira pomona, and wound infections, acute metritis, and traumatic injury caused by a variety of bacterial organisms (such as streptococcal and staphylococcal organisms.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day (6 to 10 mL per 100 pounds of body weight) by intramuscular injection. For leptospirosis, severe foot rot and severe forms of the indicated diseases, 5 milligrams per pound of body weight per day. Treatment should be continued 24 to 48 hours following remission of disease symptoms, not to exceed a total of 4 consecutive days.

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: No use class stated or implied • Sows with litters or about to farrow • Beef • Calves, excluding veal calves • Dairy, non-lactating
Composition / specifications
Each milliliter of sterile solution contains 100 milligrams of oxytetracycline as oxytetracycline hydrochloride.
Cattle (beef and nonlactating dairy, beef and dairy calves [excluding veal calves])
Indication

Treatment of pneumonia and shipping fever complex associated with Pasteurella spp., Haemophilus spp., and Klebsiella spp.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day (3 to 5 mL per 100 pounds of body weight) by intramuscular, subcutaneous, or intravenous injection. Treatment should be continued 24 to 48 hours following
remission of disease symptoms, not to exceed a total of 4 consecutive days.

Limitations
Swine
Indication

For treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli, pneumonia caused by Pasteurella multocida, and leptospirosis caused by Leptospira pomona.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day by intramuscular or intravenous injection.

Limitations
Swine (Sows)
Indication

As an aid in control of porcine colibacillosis (baby pig scours) in suckling pigs caused by Escherichia coli.

Dosage

3 milligrams of oxytetracycline per pound of body weight by intramuscular injection, approximately 8 hours before farrowing or immediately after completion of farrowing.

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: No use class stated or implied • Sows • Beef And Non-Lactating Dairy
Composition / specifications
Each milliliter of sterile solution contains 50 milligrams of oxytetracycline (as oxytetracycline hydrochloride).
Cattle (beef and nonlactating dairy)
Indication

Treatment of pneumonia and shipping fever complex associated with Pasteurella sp., Hemophilus sp., and Klebsiella sp., foot rot and diphtheria caused by Spherophorus necrophorus, bacterial enteritis (scours) caused by Escherichia coli, wooden tongue caused by Actinobacillus lignieresi, leptospirosis caused by Leptospira pomona, acute metritis, anaplasmosis caused by Anaplasma marginale, and wound infections caused by Staphylococcal and Streptococcal organisms.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day (6 to 10 mL per 100 pounds of body weight) by intramuscular or intravenous injection. In severe forms of foot rot, anaplasmosis, and other severe disease forms, 5 milligrams per pound of body weight per
day (10 mL per 100 pounds of body weight). Treatment should be continued 24 to 48 hours following remission of
disease symptoms, not to exceed a total of 4 days.

Limitations
Swine
Indication

For treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli, pneumonia caused by Pasteurella multocida, and leptospirosis caused by Leptospira pomona.

Dosage

3 to 5 milligrams of oxytetracycline per pound of body weight per day (6 to 10 mL per 100 pounds of body weight) by intramuscular injection.

Limitations
Swine (Sows)
Indication

As an aid in control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.

Dosage

3 milligrams of oxytetracycline per pound of body weight (6 mL per 100 lbs. body weight), by intramuscular injection, approximately 8 hours before farrowing or immediately after completion of farrowing.

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: Pacific Salmon, Reared • Freshwater-Reared Salmonids • Catfish, Reared • Freshwater-reared salmonids weighing up to 55 grams • Lobster
Composition / specifications
Type A medicated articles: 100 grams per pound. The amount of mono-alkyl (C8-C18) trimethylammonium oxytetracycline expressed is expressed in terms of an equivalent amount of oxytetracycline hydrochloride or the amount of oxytetracycline dihydrate base is expressed in terms of an equivalent amount of oxytetracycline hydrochloride.
Pacific Salmon
Indication
For marking of skeletal tissue.
Dosage

250 milligrams of Oxytetracycline per kilogram of fish per day (11.35 grams per 100 pounds of fish per day) in fish feed.

Limitations

For salmon not over 30 grams body weight. Administer as sole ration for 4 consecutive days. 

Freshwater-reared salmonids
Indication

Control of ulcer disease caused by Haemophilus piscium, furunculosis caused by Aeromonas salmonicida, bacterial hemorrhagic septicemia caused by Aeromonas hydrophila, and pseudomonas disease.

Dosage
2.5 to 3.75 grams Oxytetracycline per 100 pounds of fish per day in fish feed.
Limitations

Administer in mixed ration for 10 days. 

Catfish
Indication

Control of bacterial hemorrhagic septicemia caused by Aeromonas hydrophila and pseudomonas disease.

Dosage
2.5 to 3.75 grams Oxytetracycline per 100 pounds of fish per day in fish feed.
Limitations

Administer in mixed ration for 10 days. Do not administer when water temperature is below 16.7 degrees C (62 degrees F).

Freshwater-reared salmonids
Indication
Control of mortality due to coldwater disease associated with Flavobacterium psychrophilum.
Dosage

3.75 g oxytetracycline per 100 lb of fish per day for 10 days.

Limitations

Administer in mixed ration for 10 days. 

Freshwater-reared salmonids
Indication

Control of mortality due to columnaris disease associated with Flavobacterium columnare.

Dosage

3.75 g oxytetracycline per 100 lb of fish per day for 10 days.

Limitations

Administer in mixed ration for 10 days. 

Lobster
Indication
Control of gaffkemia caused by Aerococcus viridans.
Dosage
1 gram Oxytetracycline per pound of medicated feed in fish feed.
Limitations
Administer as sole ration for 5 consecutive days.
Freshwater-reared salmonids weighing up to 55 grams
Indication

For marking the skeletal tissue

Dosage

3.75 g oxytetracycline per 100 lb of fish per day for 10 days. Feed for 10 days.

Limitations
Catfish
Indication

Control of mortality due to columnaris disease associated with Flavobacterium columnare

Dosage

3.75 g oxytetracycline per 100 lb of fish per day for 10 days. Administer in mixed ration for 10 days. Do not administer when water temperature is below 16.7 degrees C (62 degrees F).

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: Breeding • No use class stated or implied • Growing • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption
Composition / specifications
Each 2.73 grams of powder contains 1 gram of oxytetracycline hydrochloride (packets: 9.87 oz, 3.09 lb and 3.91 lb)
Chickens
Indication

Control of chronic respiratory disease (CRD) and air sac infections caused by Mycoplasma gallisepticum and E. coli susceptible to oxytetracycline; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

400 to 800 milligrams per gallon of drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Indication

Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage

200 to 400 milligrams per gallon of drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Turkeys
Indication

Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage

400 milligrams per gallon of drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Indication

Control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.

Dosage

200 to 400 milligrams per gallon of drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Turkeys (growing)
Indication

Control of complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis) susceptible to oxytetracycline.

Dosage

25 milligrams per pound of body weight in drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Swine
Indication

Control and treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily in drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Use as sole source of OTC. Administer up to 5 days. Do not use for more than 5 consecutive days.

Swine (breeding stock)
Indication

Control and treatment of leptospirosis (reducing the incidence of abortions and shedding of leptospira) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily in drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Use as sole source of OTC. Administer up to 5 days. Do not use for more than 5 consecutive days.

FDA page: Open in Animal Drugs @ FDA

Species: No use class stated or implied • Sows • Calves, Including Prerumenative Veal • Beef • Dairy, non-lactating
Composition / specifications
Each mL of solution contains 300 mg oxytetracycline base.
Beef Cattle, Non-lactating Dairy Cattle, and Calves including Pre-ruminating (Veal) Calves
Indication

For treatment of bacterial pneumonia caused by Pasteurella species (shipping fever) in calves and yearlings where treatment is impractical due to husbandry conditions, such as cattle on range, or where their repeated restraint is inadvisable; or for treatment of infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis.

Dosage

9 to 13.6 milligrams per pound of body weight. Administer once intramuscularly or subcutaneously.

Limitations
Indication

For control of respiratory disease in cattle at high risk of developing bovine respiratory disease associated with Mannheimia (Pasteurella) haemolytica.

Dosage

13.6 milligrams per pound of body weight. Administer once intramuscularly or subcutaneously.

Limitations
Indication

For treatment of pneumonia and shipping fever complex associated with Pasteurella species and Histophilus species, foot-rot and diphtheria caused by Fusobacterium necrophorum, bacterial enteritis (scours) caused by Escherichia coli, wooden tongue caused by Actinobacillus lignieresii, leptospirosis caused by Leptospira pomona, and wound infections and acute metritis caused by strains of staphylococcal and streptococcal organisms sensitive to oxytetracycline.

Dosage

3 to 5 milligrams per pound of body weight per day. For treatment of severe foot-rot and advanced cases of other indicated diseases, 5 milligrams per pound of body weight per day. Administer intramuscularly, subcutaneously, or intravenously. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days.

Limitations
Swine
Indication

For treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli, pneumonia caused by Pasteurella multocida, and leptospirosis caused by Leptospira pomona.

Dosage

3 to 5 milligrams per pound of body weight per day. Administer intramuscularly. Treatment should be continued 24 to 48 hours following remission of disease signs, however, not to exceed a total of four consecutive days.

Limitations
Indication

For treatment of pneumonia caused by Pasteurella multocida where retreatment for pneumonia is impractical.

Dosage

9 milligrams per pound of body weight. Administer once intramuscularly.

Limitations
Swine (Sows)
Indication

As an aid in control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.

Dosage

3 milligrams per pound of body weight. Administer once intramuscularly approximately 8 hours before farrowing or immediately after completion of farrowing.

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: Beef • Dairy, non-lactating
Composition / specifications
Each mL contains 50 mg of oxytetracycline hydrochloride
Cattle (Beef and Non-Lactating Dairy)
Indication
Treatment of diseases due to oxytetracycline-susceptible organisms as follows: pneumonia and shipping fever complex associated with Pasteurella species and Hemophilus species; foot rot and diphtheria caused by Fusobacterium necrophorum; bacterial enteritis (scours) caused by Escherichia coli; wooden tongue caused by Actinobacillus lignieresii; leptospirosis caused by Leptospira Pomona; acute metritis and wound infections caused by staphylococcal and streptococcal organisms; if labeled for use by or on the order of a licensed veterinarian, it may be used for treatment of anaplasmosis caused by Anaplasma marginale and anthrax caused by Bacillus anthracis.
Dosage
3 to 5 milligrams per pound of body weight daily, 5 milligrams per pound for anaplasmosis, severe foot rot, and severe forms of other diseases. Administer by intravenous injection.
Limitations

Treatment should be continued 24 to 48 hours following remission of disease symptoms, but not to exceed a total of 4 consecutive days. If no improvement occurs within 24 to 48 hours, reevaluate diagnosis and therapy. Discontinue use at least 19 days prior to slaughter. This drug product is not approved for use in female dairy cattle 20months of age or older, including dry dairy cows. Use in these cattle may cause drug residues in milk and/or in calves born to these cows.

FDA page: Open in Animal Drugs @ FDA

Species: Beef • Calves • Dairy, non-lactating
Composition / specifications
Each milliliter of sterile solution contains 50 milligrams of oxytetracycline hydrochloride.
Cattle (beef, beef calves, nonlactating dairy, dairy calves)
Indication
The drug is used for treatment of bacterial pneumonia and shipping fever complex associated with Pasteurella species; foot-rot and diphtheria caused by Spherophorus necrophorus; bacterial enteritis (scours) caused by Escherichia coli; wooden tongue caused by Actinobacillus lignieresi; wound infections and acute metritis caused by staphylococcal and streptococcal organisms susceptible to oxytetracycline.
Dosage
Administer 3 to 5 milligrams of the oxytetracycline hydrochloride intramuscularly per pound of body weight per day. In severe forms of the indicated diseases, administer the equivalent of 5 milligrams of oxytetracycline hydrochloride per pound of body weight per day. Continue treatment 24 to 48 hours following remission of disease symptoms, not to exceed a total of 4 consecutive days. Reduce the volume administered per injection site according to age and body size. In calves weighing 100 pounds or less inject only 2 milliliters per site.
Limitations

If no improvement is noted within 24 to 48 hours, consult a veterinarian for diagnosis and therapy. In adult livestock, do not inject more than 10 milliliters at any one site. Rapid intravenous administration may result in animal collapse. Oxytetracycline should be administered intravenously slowly over a period of at least5 minutes.

FDA page: Open in Animal Drugs @ FDA

Species: Beef • Calves • Dairy, non-lactating
Composition / specifications
Each milliliter of sterile solution contains 100 milligrams of oxytetracycline hydrochloride.
Cattle (beef and nonlactating dairy)
Indication
Treatment of diseases due to oxytetracycline-susceptible organisms as follows: Pneumonia and shipping fever complex associated with Pasteurella species and Hemophilus species, foot-rot and diphtheria caused by Fusobacterium necrophorum, bacterial enteritis (scours) caused by Escherichia coli, wooden tongue caused by Actinobacillus lignieresii, leptospirosis caused by Leptospira pomona, and wound infections and acute metritis caused by Staphylococcus species and Streptococcus species. If labeled for use by or on the order of a licensed veterinarian, it may be used for the treatment of anaplasmosis caused by Anaplasma marginale and anthrax caused by Bacillus anthracis.
Dosage
3 to 5 milligrams of oxytetracycline per pound of body weight per day; 5 milligrams per pound of body weight per day for treatment of anaplasmosis, severe foot-rot, and severe cases of other indicated diseases. Administer intramuscularly.
Limitations
Treatment of all diseases should be instituted early and continue for 24 to 48 hours beyond remission of disease symptoms but not to exceed a total of 4 consecutive days. Consult your veterinarian if no improvement is noted within 48 hours. Do not inject more than 10 milliliters per site in adult cattle, reducing the volume according to age and body size to 1 to 2 milliliters in small calves. Exceeding the highest recommended dose of 5 milligrams per pound of body weight, administering at recommended levels for more than 4 consecutive days, and/or exceeding 10 milliliters intramuscularly per injection site may result in antibiotic residues beyond the withdrawal time. Discontinue treatment at least 15 days prior to slaughter. Not for use in lactating dairy cattle.

FDA page: Open in Animal Drugs @ FDA

Species: Beef • Calves • Dairy, non-lactating
Composition / specifications
The drug contains 100 milligrams of oxytetracycline hydrochloride in each milliliter of sterile solution.
Cattle (beef and nonlactating dairy)
Indication
The drug is intended for use in the treatment of disease due to oxytetracycline-susceptible organisms in beef cattle and non-lactating dairy cattle. It is indicated in the treatment of pneumonia and shipping fever complex associated with Pasteurella species, Hemophilus species, Klebsiella species, foot-rot and diphtheria caused by Spherophorus necrophorus, bacterial enteritis (scours) caused by Escherichia coli, wooden tongue caused by Actinobacillus lignieresi, acute metritis, and wound infections caused by staphylococcal and streptococcal organisms.
Dosage
It is administered to cattle at a dosage level of 3 to 5 milligrams per pound of body weight per day. It is administered intravenously from a 100 milligram per milliliter solution. Severe foot-rot and the severe forms of the indicated diseases should be treated with 5 milligrams per pound of body weight. Treatment should be continued 24 to 48 hours following remission of disease symptoms, however, not to exceed a total of 4 consecutive days. If no improvement is noted within 24 hours consult a veterinarian. When injecting the drug intramuscularly do not inject more than 10 milliliters per site in adult cattle. Reduce the amount injected at each site according to the size of the animal. For very small calves do not use more than 2 milliliters per injection site.
Limitations
Not for use in lactating dairy cattle. Discontinue treatment at least 19 days prior to slaughter. When administered intramuscularly within 30 days of slaughter, muscle discoloration may necessitate trimming of the injection site and surrounding tissues.

FDA page: Open in Animal Drugs @ FDA

Species: No use class stated or implied • Sows with litters or about to farrow • Beef • Calves • Dairy, non-lactating
Composition / specifications
Each milliliter of sterile solution contains 100 milligrams of oxytetracycline hydrochloride.
Swine
Indication
For treatment of bacterial enteritis (scours colibacillosis) caused by Escherichia coli, pneumonia caused by Pasteurella multocida, and leptospirosis caused by Leptospira pomona.
Dosage
3 to 5 milligrams of oxytetracycline per pound of body weight per day. Administer intramuscularly.
Limitations
Do not inject more than 5 milliliters per site in adult swine, reducing the volume according to age and body size to 1 to 2 milliliters in young pigs. Discontinue treatment at least 22 days prior to slaughter.
Swine (sows with litters or about to farrow)
Indication
As an aid in control of infections enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.
Dosage
3 milligrams of oxytetracycline per pound of body weight, administered once, approximately 8 hours before farrowing or immediately after completion of farrowing. Administer intramuscularly.
Limitations
Do not inject more than 5 milliliters per site in adult swine, reducing the volume according to age and body size to 1 to 2 milliliters in young pigs. Discontinue treatment at least 22 days prior to slaughter.
Cattle (beef and nonlactating dairy)
Indication
Treatment of diseases due to oxytetracycline-susceptible organisms as follows: Pneumonia and shipping fever complex associated with Pasteurella species and Hemophilus species, foot-rot and diphtheria caused by Fusobacterium necrophorum, bacterial enteritis (scours) caused by Escherichia coli, wooden tongue caused by Actinobacillus lignieresii, leptospirosis caused by Leptospira pomona, and wound infections and acute metritis caused by Staphylococcus species and Streptococcus species If labeled for use by or on the order of a licensed veterinarian, it may be used for the treatment of anaplasmosis caused by Anaplasma marginale and anthrax caused by Bacillus anthracis.
Dosage
3 to 5 milligrams of oxytetracycline per pound of body weight per day; 5 milligrams per pound of body weight per day for treatment of anaplasmosis, severe foot-rot, and severe cases of other indicated diseases. Administer intramuscularly.
Limitations
Treatment of all diseases should be instituted early and continue for 24 to 48 hours beyond remission of disease symptoms but not to exceed a total of 4 consecutive days. Consult your veterinarian if no improvement is noted within 48 hours. Do not inject more than 10 milliliters per site in adult cattle, reducing the volume according to age and body size to 1 to 2 milliliters in small calves. Exceeding the highest recommended dose of 5 milligrams per pound of body weight, administering at recommended levels for more than 4 consecutive days, and/or exceeding 10 milliliters intramuscularly per injection site may result in antibiotic residues beyond the withdrawal time. Discontinue treatment at least 15 days prior to slaughter. Not for use in lactating dairy cattle.

FDA page: Open in Animal Drugs @ FDA

Species: Beef calves • Dairy calves
Composition / specifications
Each tablet contains 250 of oxytetracycline hydrochloride
Cattle (beef and dairy calves)
Indication

For treatment of bacterial enteritis caused by Salmonella typhimurium and Escherichia coli (colibacillosis) and bacterial pneumonia (shipping fever complex, pasteurellosis) caused by Pasteurella multocida.

Dosage

Orally administer 2 tablets per 100 lb of body weight every 12 hours (10 mg/lb of body weight daily in divided doses) for up to 4 consecutive days. Dosage should continue until the animal returns to normal and for 24-48 hours after symptoms have subsided. Treatment should not exceed 4 consecutive days.

Limitations
Indication

For control of bacterial enteritis caused by Salmonella typhimurium and Escherichia coli (colibacillosis) and bacterial pneumonia (shipping fever complex, pasteurellosis) caused by Pasteurella multocida.

Dosage

Orally administer 1 tablet per 100 lb of body weight every 12 hours (5 mg/lb of body weight daily in divided doses) for up to 4 consecutive days. Dosage should continue until the animal returns to normal and for 24-48 hours after symptoms have subsided. Treatment should not exceed 4 consecutive days.

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: Honey Bees • Breeding • No use class stated or implied • Beef • Calves • Dairy, non-lactating • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Lobster • Sheep, No Use Class Stated Or Implied
Composition / specifications
Type A medicated articles containing 50 grams oxytetracycline (from oxytetracycline quaternary salt) equivalent to oxytetracycline hydrochloride per pound
Chickens
Indication
For reduction of mortality due to air sacculitis (air-sac infection) caused by E. coli susceptible to oxytetracycline.
Dosage
500 grams per ton of feed.
Limitations

Feed continuously for 5 days. Do not administer to chickens producing eggs for human consumption. Withdraw 24 hours before slaughter. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues.

Indication
For control of chronic respiratory disease (CRD) and air sac infection caused by M. gallisepticum and Escherichia coli susceptible to oxytetracycline.
Dosage
400 grams per ton of feed.
Limitations

Feed continuously for 7 to 14 days. Do not administer to chickens producing eggs for human consumption. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues.

Indication
Control of infectious synovitis caused by Mycoplasma synoviae; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.
Dosage
100 - 200 grams per ton of feed.
Limitations

Feed continuously for 7 to 14 days. Do not administer to chickens producing eggs for human consumption. Do not use in low-calcium feed containing less than 0.55% dietary calcium. Use in such feeds may result in violative residues.

Turkeys
Indication
For control of complicating bacterial organisms associated with bluecomb (transmissible enteritis; coronaviral enteritis) susceptible to oxytetracycline.
Dosage
25 milligrams per pound of body weight.
Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not administer to turkeys producing eggs for human consumption.

Indication
For control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.
Dosage
100 grams per ton of feed.
Limitations

Feed continuously for 7 to 14 days. Do not administer to turkeys producing eggs for human consumption.

Indication
For control of infectious synovitis caused by M. synoviae susceptible to oxytetracycline.
Dosage
200 grams per ton of feed.
Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter. Do not administer to turkeys producing eggs for human consumption.

Swine
Indication
For treatment of bacterial enteritis caused by E. coli and Salmonella choleraesuis susceptible to oxytetracycline and treatment of bacterial pneumonia caused by P. multocida susceptible to oxytetracycline.
Dosage
10 milligrams per pound of body weight.
Limitations

Feed continuously for 7 to 14 days. 

Swine (Breeding)
Indication

For control and treatment of leptospirosis (reducing the incidence of abortion and shedding of leptospirae) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight.
Limitations

Feed continuously for not more than 14 days.  

Cattle (beef and non-lactating dairy: growing cattle over 400 pounds)
Indication

For the reduction of the incidence of liver abscesses.

Dosage

75 milligrams per head per day.

Limitations

Feed continuously.

Cattle (calves including veal calves, beef, and non-lactating dairy)
Indication

Treatment of bacterial enteritis caused by E. coli.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. In milk replacer or starter feed. Withdraw 0 days before slaughter. When used in milk replacers, the treatment claim (10 mg/lb) is limited to bacterial enteritis caused by E. coli only.

Indication

Treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline).

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Withdraw 0 days before slaughter.

Indication
For prevention and treatment of the early stages of shipping fever complex.
Dosage
0.5 - 2.0 grams per head per day in feed.
Limitations

Feed 3 to 5 days before and after arrival in feedlots. 

Sheep
Indication

For treatment of bacterial enteritis caused by E. coli and bacterial pneumonia caused by P. multocida susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight daily.

Limitations

Feed continuously for 7 to 14 days. Withdraw 5 days before slaughter.

Lobsters
Indication
For control of gaffkemia caused by Aerococcus viridans.
Dosage
1 gram per pound medicated feed.
Limitations

Administer as sole ration for 5 consecutive days. Withdraw medicated feed 30 days before harvesting lobsters.

Honey bees
Indication

Control of American Foulbrood caused by Bacillus larvae, and European foulbrood caused by Streptococcus pluton susceptible to oxytetracycline.

Dosage

200 milligrams per colony.

Limitations

Remove at least 6 weeks prior to main honey flow.

FDA page: Open in Animal Drugs @ FDA

Species: Fish, Finfish, Fry And Fingerlings
Composition / specifications
Each gram of soluble powder contains 366 milligrams (mg) of oxytetracycline hydrochloride.
Finfish
Indication
For skeletal marking of finfish fry and fingerlings.
Dosage
Immerse fish in a solution containing 200 to 700 mg oxytetracycline hydrochloride (buffered) per liter of water for 2 to 6 hours.
Limitations

FDA page: Open in Animal Drugs @ FDA

Species: Honey Bees • Breeding • No use class stated or implied • Beef • Calves • Dairy, females Under 20 months of age • Growing • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Sheep, No Use Class Stated Or Implied
Composition / specifications
Each 18.1 grams of powder contains 1 gram of oxytetracycline hydrochloride (packet: 6.4 oz; pails: 2 and 5 lb)
Chickens
Indication

Control of chronic respiratory disease (CRD) and air sac infections caused by Mycoplasma gallisepticum and E. coli susceptible to oxytetracycline; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage
400 to 800 milligrams per gallon of drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Indication

Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage

200 to 400 milligrams per gallon of drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Turkeys
Indication

Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage
400 milligrams per gallon of drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of oxytetracycline. Use as a sole source of drinking water. Do not use in birds producing eggs for human consumption. Withdraw 5 days prior to slaughter.

Indication

Control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.

Dosage

200 - 400 milligrams per gallon of drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of oxytetracycline. Use as a sole source of drinking water. Do not use in birds producing eggs for human consumption. Withdraw 5 days prior to slaughter.

Turkeys (growing)
Indication
Control of complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis) susceptible to oxytetracycline.
Dosage

25 milligrams per pound of body weight.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of oxytetracycline. Use as a sole source of drinking water. Do not use in birds producing eggs for human consumption. Withdraw 5 days prior to slaughter.

Swine
Indication

Control and treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight in drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Zero-day slaughter withdrawal in swine.

Swine (breeding stock)
Indication

Control and treatment of leptospirosis (reducing the incidence of abortions and shedding of leptospira) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Zero–day slaughter withdrawal in swine.

Cattle (calves, beef and nonlactating dairy)
Indication

Control and treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight in drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as sole source of oxytetracycline. Do not administer this product with milk or milk replacers. Administer 1 hour before or 2 hours after feeding milk or milk replacers. Withdraw 5 days prior to slaughter. A milk discard period has not been established for this product in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older.

Sheep
Indication

Control and treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight in drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Withdraw 5 days prior to slaughter.

Honey bees
Indication

Control of American foul brood caused by Paenibacillus larvae susceptible to oxytetracycline.

Dosage

200 milligrams per colony, administered via either an 1:1 sugar syrup (equal parts of sugar and water weight to weight) or dusting with a powdered sugar mixture.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. The drug is administered in 3 applications of sugar syrup or 3 dustings at 4- to 5- days intervals. The drug should be fed early in the spring or fall and consumed by the bees before main honey flow begins to avoid contamination of production honey. Remove at least 6 weeks prior to main honey flow. Dusting of uncapped brood cells has been reported to cause death of larval honey bees. Do not dust uncapped brood cells.

FDA page: Open in Animal Drugs @ FDA

Species: Honey Bees • Fish, Finfish, Fry And Fingerlings • Breeding • No use class stated or implied • Beef • Calves • Dairy, females Under 20 months of age • Growing • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Sheep, No Use Class Stated Or Implied
Composition / specifications
Each 1.32 grams of powder contains 1 gram of OTC HCl (packet: 4.78 ounce and 9.6 ounce; pails 2 and 5 pounds)
Chickens
Indication

Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage
200 to 400 milligrams per gallon of drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Indication

Control of chronic respiratory disease (CRD) and air sac infections caused by Mycoplasma gallisepticum and E. coli susceptible to oxytetracycline; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage
400 to 800 milligrams per gallon of drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Turkeys
Indication

For the control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.

Dosage

200 – 400 milligrams per gallon of drinking water.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of oxytetracycline. Use as a sole source of drinking water. Do not use in birds producing eggs for human consumption. Withdraw 5 days before slaughter.

Indication

Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage
400 milligrams per gallon of drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of oxytetracycline. Use as a sole source of drinking water. Do not use in birds producing eggs for human consumption. Withdraw 5 days before slaughter.

Turkeys (growing)
Indication

Control of complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis) susceptible to oxytetracycline.

Dosage
25 milligrams per pound of body weight in drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of oxytetracycline. Use as a sole source of drinking water. Do not use in birds producing eggs for human consumption. Withdraw 5 days before slaughter.

Swine
Indication

Control and treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight in drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Zero-day slaughter withdrawal in swine.

Swine (breeding stock)
Indication

Control and treatment of leptospirosis (reducing the incidence of abortions and shedding of leptospira) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Zero–day slaughter withdrawal in swine.

Cattle (calves, beef, and nonlactating dairy)
Indication

Control and treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight in drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as sole source of oxytetracycline. Do not administer this product with milk or milk replacers. Administer 1 hour before or 2 hours after feeding milk or milk replacers. Withdraw 5 days prior to slaughter. A milk discard period has not been established for this product in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older.

Sheep
Indication

Control and treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight in drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Withdraw 5 days prior to slaughter.

Honey bees
Indication

Control of American foul brood caused by Paenibacillus larvae susceptible to oxytetracycline.

Dosage

200 milligrams per colony, administered via either a 1:1 sugar syrup (equal parts of sugar and water weight to weight) or dusting with a powdered sugar mixture.

Limitations
Finfish fry and fingerlings
Indication
For skeletal marking of finfish fry and fingerlings.
Dosage

Immerse fish in a solution containing 200 to 700 mg oxytetracycline hydrochloride (buffered) per liter of water for 2 to 6 hours.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

FDA page: Open in Animal Drugs @ FDA

Species: Fish, Finfish, Fry And Fingerlings
Composition / specifications
Each 2.73 grams of powder contains 1 gram of OTC HCl (packets: 2.46 and 9.87 ounce; pail: 3.09 pound). Each gram of powder contains 366 milligrams (mg) of oxytetracycline hydrochloride.
Finfish
Indication
For skeletal marking of finfish fry and fingerlings
Dosage

Immerse fish in a solution containing 200 to 700 mgoxytetracycline hydrochloride (buffered) per liter of water for 2 to 6 hours.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian

FDA page: Open in Animal Drugs @ FDA

Species: Breeding • No use class stated or implied • Growing • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption
Composition / specifications
4.78 oz. (135.5 g) pouch: each packet contains 102.4 grams of oxytetracycline hydrochloride. 5 lb. (2.27 kg) pail: each pail contains 1.715 kilograms of oxytetracycline hydrochloride. 3.09 lb. (1400 g) pouch: each packet contains 512 grams of oxytetracycline hydrochloride. 9.87 oz. (280 g) packet: each packet contains 102.4 grams of oxytetracycline hydrochloride
Chickens
Indication

For the control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage

Administer 200 to 400 milligrams of powder per gallon of drinking water.

Limitations

Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption. Use as the sole source of oxytetracycline. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Indication

For the control of chronic respiratory disease (CRD) and air sac infections caused by Mycoplasma gallisepticum and E. coli susceptible to oxytetracycline; for the control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

Administer 400 to 800 milligrams of powder per gallon of drinking water.

Limitations

Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption. Use as the sole source of oxytetracycline. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Turkeys
Indication

For the control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.

Dosage

Administer 200 to 400 milligrams of powder per gallon of drinking water.

Limitations

Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption. Use as the sole source of oxytetracycline. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Indication

For the control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Dosage

Administer 400 milligrams of powder per gallon of drinking water.

Limitations

Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption. Use as the sole source of oxytetracycline. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Turkeys (growing)
Indication

For the control of complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis) susceptible to oxytetracycline.

Dosage

Administer 25 milligrams per pound of body weight in drinking water.

Limitations

Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption. Use as the sole source of oxytetracycline. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Swine
Indication

For the control and treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage

Administer 10 milligrams per pound of body weight daily in drinking water.

Limitations

Prepare a fresh solution daily. Use as the sole source of oxytetracycline. Administer up to 5 days; do not use for more than 5 consecutive days. Use as sole source of drinking water. Do not mix this product directly with milk or milk replacers. Administer one hour before or two hours after feeding milk or milk replacers. Withdraw zero days prior to slaughter. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Swine (breeding stock)
Indication

For the control and treatment of leptospirosis (reducing the incidence of abortions and shedding of leptospira) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage

Administer 10 milligrams per pound of body weight daily in drinking water.

Limitations

Prepare a fresh solution daily. Use as the sole source of oxytetracycline. Administer up to 5 days; do not use for more than 5 consecutive days. Use as sole source of drinking water. Do not mix this product directly with milk or milk replacers. Administer one hour before or two hours after feeding milk or milk replacers. Withdraw zero days prior to slaughter. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

FDA page: Open in Animal Drugs @ FDA

Species: Growing • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption
Composition / specifications
Each 4.2 gram of powder contains 1 gram of oxytetracycline hydrochloride.
Chickens
Indication

Control of chronic respiratory disease (CRD) and air sac infections caused by Mycoplasma gallisepticum and E. coli and fowl cholera caused by Pasteurella multocida.

Dosage

400 to 800 milligrams per gallon of drinking water. 

Limitations

Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Indication
Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.
Dosage

200 to 400 milligrams per gallon of drinking water. 

Limitations

Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Turkeys
Indication
Control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.
Dosage

200 to 400 milligrams per gallon of drinking water. 

Limitations

Administer for 7 to 14 days; do not slaughter for food within 4 days of treatment; not for use in turkeys producing eggs for human consumption; prepare a fresh solution daily; use as the sole source of tetracycline.

Indication
Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.
Dosage

400 milligrams per gallon of drinking water. 

Limitations

Administer for 7 to 14 days; do not slaughter for food within 4 days of treatment; not for use in turkeys producing eggs for human consumption; prepare a fresh solution daily; use as the sole source of tetracycline.

Indication

Control of complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis).

Dosage

25 mg/lb of body weight per day in drinking water.

Limitations

Administer for 7 to 14 days; do not slaughter for food within 4 days of treatment; not for use in turkeys producing eggs for human consumption; prepare a fresh solution daily; use as the sole source of tetracycline.

FDA page: Open in Animal Drugs @ FDA

Species: Honey Bees • Fish, Finfish, Fry And Fingerlings • Breeding • No use class stated or implied • Beef • Calves • Dairy, females Under 20 months of age • Growing • Not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption • Sheep, No Use Class Stated Or Implied
Composition / specifications
Each 677.5 gram packet contains 512 grams of oxytetracycline hydrochloride (OTC HCL)(packet 23.9 oz).
Chickens
Indication
Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.
Dosage
200 to 400 milligrams per gallon of drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Indication
Control of chronic respiratory disease (CRD) and air sac infections caused by Mycoplasma gallisepticum and E. coli susceptible to oxytetracycline; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.
Dosage
400 to 800 milligrams per gallon of drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

Turkeys
Indication

Control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.

Dosage
200 - 400 milligrams per gallon of drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of oxytetracycline. Use as a sole source of drinking water. Do not use in birds producing eggs for human consumption. Zero day slaughter withdrawal in turkeys.

Indication
Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.
Dosage
400 milligrams per gallon of drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of oxytetracycline. Use as a sole source of drinking water. Do not use in birds producing eggs for human consumption. Zero day slaughter withdrawal in turkeys.

Turkeys (growing)
Indication
Control of complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis) susceptible to oxytetracycline.
Dosage

25 milligrams per pound of body weight.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of oxytetracycline. Use as a sole source of drinking water. Do not use in birds producing eggs for human consumption. Zero day slaughter withdrawal in turkeys.

Swine
Indication

Control and treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.

Dosage
10 milligrams per pound of body weight daily in drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Administer up to 5 days. Do not use for more than 5 consecutive days. Zero day slaughter withdrawal in swine.

Cattle (calves, beef, and nonlactating dairy)
Indication
Control and treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline.
Dosage
10 milligrams per pound of body weight daily in drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer up to 5 days. Do not use for more than 5 consecutive days. Use as sole source of oxytetracycline. Do not administer this product with milk or milk replacers. Administer 1 hour before or 2 hours after feeding milk or milk replacers. Withdraw 5 days prior to slaughter. A milk discard period has not been established for this product in lactating dairy cattle. Do not use in female dairy cattle 20 months of age or older.

Swine (breeding stock)
Indication

Control and treatment of leptospirosis (reducing the incidence of abortions and shedding of leptospira) caused by Leptospira pomona susceptible to oxytetracycline.

Dosage

10 milligrams per pound of body weight.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Administer up to 5 days. Do not use for more than 5 consecutive days. Zero day slaughter withdrawal in swine.

Sheep
Indication
Control and treatment of bacterial enteritis caused by E. coli and bacterial pneumonia (shipping fever complex) caused by P. multocida susceptible to oxytetracycline.
Dosage
10 milligrams per pound of body weight in drinking water.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer up to 5 days. Do not use for more than 5 consecutive days. Use as a sole source of oxytetracycline. Withdraw 5 days prior to slaughter.

Honey Bees
Indication

Control of American foul brood caused by Paenibacillus larvae susceptible to oxytetracycline.

Dosage
200 milligrams per colony, administered via either a 1:1 sugar syrup (equal parts of sugar and water weight to weight) or dusting with a powdered sugar mixture.
Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. The drug is administered in 3 applications of sugar syrup or 3 dustings at 4- to 5- days intervals. The drug should be fed early in the spring or fall and consumed by the bees before main honey flow begins to avoid contamination of production honey. Remove at least 6 weeks prior to main honey flow. Dusting of uncapped brood cells has been reported to cause death of larval honey bees. Do not dust uncapped brood cells.

Finfish fry and fingerlings
Indication

For skeletal marking of finfish fry and fingerlings.

Dosage

Immerse fish in a solution containing 200 to 700 mg oxytetracycline hydrochloride (buffered) per liter of water for 2 to 6 hours.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian. For skeletal marking of finfish fry and fingerlings.

FDA page: Open in Animal Drugs @ FDA

Species: Cattle, Dairy, Not Lactating • Swine, No Use Class Stated Or Implied • Swine, Sows With Litters Or About To Farrow • Cattle, Beef
Composition / specifications
200 milligrams/milliliter
Sows
Indication
As an aid in control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by E. coli.
Dosage
3 milligrams per pound of body weight intramuscularly once.
Limitations
Administer intramuscularly. Do not inject more than 5 mL per site in adult swine. Discontinue treatment at least 28 days prior to slaughter.
Swine
Indication
Where re-treatment for pneumonia is impractical.
Dosage
9 milligrams per pound of body weight as a single dosage.
Limitations
Administer intramuscularly. Do not inject more than 5 mL per site in adult swine. Discontinue treatment at least 28 days prior to slaughter.
Indication
For treatment of bacterial enteritis (scours, colibacillosis) caused by E. coli, pneumonia caused by Pasteurella multocida, and leptospirosis caused by Leptospira pomona.
Dosage
3 to 5 milligrams of oxytetracycline per pound of body weight per day.
Limitations
Administer intramuscularly. Do not inject more than 5 mL per site in adult swine. Discontinue treatment at least 28 days prior to slaughter.
Cattle (beef,dairy excluding lactating animals, and calves, including preruminating veal calves)
Indication
Where retreatment of calves and yearlings for bacterial pneumonia is impractical, for treatment of infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis, or where retreatment for anaplasmosis is impractical.
Dosage
9 milligrams per pound of body weight intramuscularly or subcutaneously as a single dose.
Limitations
Administer intramuscularly or intravenously. Exceeding the highest recommended level of drug per pound of bodyweight per day, administering more than the recommended number of treatments, and/or exceeding 10 mL intramuscularly or subcutaneously per injection site may result in antibiotic residues beyond the withdrawal time. Rapid intravenous administration in cattle may result in animal collapse. Oxytetracycline should be administered intravenously slowly over a period of at least 5 minutes. Discontinue treatment at least 28 days prior to slaughter. Not for use in lactating dairy animals. Federal law restricts this drug to use by or on the order of a licensed veterinarian.
Indication
For treatment of anaplasmosis, severe foot-rot and advanced cases of other indicated diseases.
Dosage
5 milligrams per pound of body weight per day.
Limitations
Administer intramuscularly, subcutaneously, or intravenously. Exceeding the highest recommended level of drug per pound of bodyweight per day, administering more than the recommended number of treatments, and/or exceeding 10 mL intramuscularly or subcutaneously per injection site may result in antibiotic residues beyond the withdrawal time. Rapid intravenous administration in cattle may result in animal collapse. Oxytetracycline should be administered intravenously slowly over a period of at least 5 minutes. Discontinue treatment at least 28 days prior to slaughter. Not for use in lactating dairy animals.
Indication
For treatment of pneumonia and shipping fever complex associated with Pasteurella species and Haemophilus species, foot-rot and diphtheria caused by Fusobacterium necrophorum, bacterial enteritis (scours) caused by Escherichia coli, wooden tongue caused by Actinobacillus lignieresii, leptospirosis caused by Leptospira pomona, wound infections and acute metritis caused by Staphylococcus species and Streptococcus species, and anthrax caused by Bacillus anthracis.
Dosage
3 to 5 milligrams of oxytetracycline per pound of body weight per day.
Limitations
Administer intramuscularly, subcutaneously, or intravenously. Exceeding the highest recommended level of drug per pound of bodyweight per day, administering more than the recommended number of treatments, and/or exceeding 10 mL intramuscularly or subcutaneously per injection site may result in antibiotic residues beyond the withdrawal time. Rapid intravenous administration in cattle may result in animal collapse. Oxytetracycline should be administered intravenously slowly over a period of at least 5 minutes. Discontinue treatment at least 28 days prior to slaughter. Not for use in lactating dairy animals. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

FDA page: Open in Animal Drugs @ FDA

Species: No use class stated or implied • Sows with litters or about to farrow • Beef • Dairy, non-lactating • Breeders not laying eggs for human consumption • Broilers not laying eggs for human consumption • Excluding turkeys producing eggs for human consumption
Composition / specifications
The drug contains 50 milligrams of oxytetracycline hydrochloride in each milliliter of sterile solution.
Cattle (beef and nonlactating dairy)
Indication
It is used for the treatment of pneumonia and shipping fever complex associated with Pasteurella species and Hemophilus species; foot-rot and diphtheria caused by Spherophorus necrophorus; bacterial enteritis (scours) caused by Escherichia coli; wooden tongue caused by Actinobacillus lignieresi; leptospirosis caused by Leptospira pomona; wound infections and acute metritis caused by staphylococcal and streptococcal organisms.
Dosage
Administer by intravenous or intramuscular injection at 3 to 5 milligrams of oxytetracycline per pound of body weight per day. In the treatment of severe foot-rot and severe forms of the indicated diseases, a dosage level of 5 milligrams per pound of body weight per day is recommended. If the labeling of the drug bears the statement ``Federal law restricts this drug to use by or on the order of a licensed veterinarian,'' it may include additional directions for use in beef cattle and nonlactating dairy cattle for the treatment of anaplasmosis caused by Anaplasma marginale and anthrax caused by Bacillus anthracis in which case the drug is given at 3 to 5 milligrams of oxytetracycline per pound of body weight per day for anthrax, and at 5 milligrams per pound of body weight per day for anaplasmosis.
Limitations
Treatment of all diseases should be instituted early. Treatment should continue for 24 to 48 hours beyond the remission of disease symptoms, but not exceed a total of 4 consecutive days. If no improvement is noted within 24 to 48 hours, diagnosis and therapy should be reevaluated. When injecting intramuscularly in adult livestock, do not inject more than 10 milliliters at any one site. The volume administered per injection site should be reduced according to age and body size so that 1 or 2 milliliters are injected in smaller animals such as small calves. Intravenous administration is recommended in cattle when daily dosage exceeds 50 milliliters. Treatment must be discontinued at least 22 days prior to slaughter for cattle. When administered intramuscularly to animals within 30 days of slaughter, muscle discoloration may necessitate trimming of the injection site(s) and surrounding tissues during the dressing procedure. Not for use in lactating dairy animals.
Swine
Indication
It is used for the treatment of bacterial enteritis (scours, colibacillosis) caused by Escherichia coli; pneumonia caused by Pasteurella multocida; and leptospirosis caused by Leptospira pomona.
Dosage
Administer by intramuscular injection at 3 to 5 milligrams of oxytetracycline per pound of body weight per day to swine.
Limitations
Treatment of all diseases should be instituted early. Treatment should continue for 24 to 48 hours beyond the remission of disease symptoms, but not exceed a total of 4 consecutive days. If no improvement is noted within 24 to 48 hours, diagnosis and therapy should be reevaluated. When injecting intramuscularly in adult livestock, do not inject more than 10 milliliters at any one site. The volume administered per injection site should be reduced according to age and body size so that 1 or 2 milliliters are injected in smaller animals such as young pigs. Treatment must be discontinued at least 22 days prior to slaughter for swine. When administered intramuscularly to animals within 30 days of slaughter, muscle discoloration may necessitate trimming of the injection site(s) and surrounding tissues during the dressing procedure.
Swine (sows about to farrow or just farrowed).
Indication
Administered to sows as an aid in the control of infectious enteritis (baby pig scours, colibacillosis) in suckling pigs caused by Escherichia coli.
Dosage
Administered to sows at 3 milligrams of oxytetracycline per pound of body weight approximately 8 hours before farrowing or immediately after farrowing. Administer intramuscularly.
Limitations
Treatment of all diseases should be instituted early. Treatment should continue for 24 to 48 hours beyond the remission of disease symptoms, but not exceed a total of 4 consecutive days. If no improvement is noted within 24 to 48 hours, diagnosis and therapy should be reevaluated. When injecting intramuscularly in adult livestock, do not inject more than 10 milliliters at any one site. The volume administered per injection site should be reduced according to age and body size so that 1 or 2 milliliters are injected in smaller animals such as young pigs. Treatment must be discontinued at least 22 days prior to slaughter for swine. When administered intramuscularly to animals within 30 days of slaughter, muscle discoloration may necessitate trimming of the injection site(s) and surrounding tissues during the dressing procedure.
Chickens (broilers and breeding chickens)
Indication
It is used for the treatment of air sacculitis (air-sac disease chronic respiratory disease) caused by Mycoplasma gallisepticum and Escherichia coli; fowl cholera caused by Pasteurella multocida; infectious sinusitis caused by Mycoplasma gallisepticum; and infectious synovitis caused by Mycoplasma synoviae.
Dosage
Administered subcutaneously to chickens 1 day to 2 weeks of age at 6.25 milligrams of oxytetracycline per bird per day diluted with 1 part of the drug to 3 parts of sterile water; to chickens 2 to 4 weeks of age using the same diluted product at 12.5 milligrams of oxytetracycline per bird; to chickens 4 to 8 weeks of age without dilution at 25 milligrams of oxytetracycline per bird; to chickens 8 weeks of age (broilers and light pullets) at 50 milligrams of oxytetracycline per bird; to adult chickens at 100 milligrams of oxytetracycline per bird.
Limitations
Treatment of all diseases should be instituted early. Treatment should continue for 24 to 48 hours beyond the remission of disease symptoms, but not exceed a total of 4 consecutive days. If no improvement is noted within 24 to 48 hours, diagnosis and therapy should be reevaluated. Treatment must be discontinued at least 5 days prior to slaughter for chickens. Do not administer to laying hens unless the eggs are used for hatching only.
Turkeys
Indication
It is used for the treatment of air sacculitis (air-sac disease chronic respiratory disease) caused by Mycoplasma gallisepticum and Escherichia coli; fowl cholera caused by Pasteurella multocida; infectious sinusitis caused by Mycoplasma gallisepticum; and infectious synovitis caused by Mycoplasma synoviae.
Dosage
Administered subcutaneously to turkeys 1 day to 2 weeks of age and 2 to 4 weeks of age at the same dosage as chickens; to turkeys 4 to 6 weeks of age at 50 milligrams of oxytetracycline as the undiluted product per bird; to turkeys 6 to 9 weeks of age at 100 milligrams of oxytetracycline per bird; to turkeys 9 to 12 weeks of age at 150 milligrams of oxytetracycline per bird; to turkeys 12 weeks of age and older at 200 milligrams of oxytetracycline per bird. In light turkey breeds, no more than 25 milligrams per pound of body weight is administered. For the treatment of infectious sinusitis in turkeys, 1/4 to 1/2 milliliter of the drug is injected directly into each swollen sinus depending upon the age of the bird and the severity of the condition. At the time that the sinuses are treated, the drug should also be administered subcutaneously to the birds according to the dosage schedule stated above for chickens and turkeys. If refilling of the sinuses occurs, the treatment may be repeated in 5 to 7 days.
Limitations
Treatment of all diseases should be instituted early. Treatment should continue for 24 to 48 hours beyond the remission of disease symptoms, but not exceed a total of 4 consecutive days. If no improvement is noted within 24 to 48 hours, diagnosis and therapy should be reevaluated. Treatment must be discontinued at least 5 days prior to slaughter for turkeys. Do not administer to laying hens unless the eggs are used for hatching only.

FDA page: Open in Animal Drugs @ FDA

Species: Swine, Breeding Swine • Swine, No Use Class Stated Or Implied • Turkey, Growing • Turkey, Not Laying Eggs For Human Consumption • Chicken, Not Laying Eggs For Human Consumption
Composition / specifications
The drug is a soluble powder distributed in packets (9.87oz and 19.47oz) or pails (5lb). Each 2.73 grams of powder contains 1 gram of oxytetracycline hydrochloride.
Swine (breeding stock)
Indication
Control and treatment of leptospirosis (reducing the incidence of abortions and shedding of leptospira) caused by Leptospira pomona susceptible to oxytetracycline.
Dosage
10 milligrams per pound of body weight daily in drinking water.
Limitations
Prepare a fresh solution daily. Use as sole source of OTC. Administer up to 5 days. Do not use for more than 5 consecutive days.
Turkeys (growing)
Indication
Control of complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis) susceptible to oxytetracycline.
Dosage
25 milligrams per pound of body weight in drinking water.
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.
Swine
Indication
Control and treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis and bacterial pneumonia caused by Pasteurella multocida susceptible to oxytetracycline.
Dosage
10 milligrams per pound of body weight daily in drinking water.
Limitations
Prepare a fresh solution daily. Use as sole source of OTC. Administer up to 5 days. Do not use for more than 5 consecutive days.
Chickens
Indication
Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.
Dosage
200 to 400 milligrams per gallon of drinking water.
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.
Indication
Control of chronic respiratory disease (CRD) and air sac infections caused by Mycoplasma gallisepticum and E. coli susceptible to oxytetracycline; control of fowl cholera caused by Pasteurella multocida susceptible to oxytetracycline.
Dosage
400 to 800 milligrams per gallon of drinking water.
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.
Turkeys
Indication
Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.
Dosage
400 milligrams per gallon of drinking water.
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.
Indication
Control of hexamitiasis caused by Hexamita meleagridis susceptible to oxytetracycline.
Dosage
200 to 400 milligrams per gallon of drinking water.
Limitations
Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption.

FDA page: Open in Animal Drugs @ FDA

Species: Chicken, Broilers
Composition / specifications
Type A medicated articles: 10, 20, 30, 40, 50, 100, and 200 grams per pound.
Chickens (broilers)
Indication
As an aid in the reduction of mortality due to air-sacculitis (air-sac-infection) caused by Escherichia coli sensitive to oxytetracycline.
Dosage
500 grams per ton of feed.
Limitations
Feed for 5 days as sole ration. Treat at first clinical signs of disease. Do not feed to laying hens. Withdraw 24 hours prior to slaughter.

FDA page: Open in Animal Drugs @ FDA

Species: Dog, No Use Class Stated Or Implied • Cat, No Use Class Stated Or Implied
Composition / specifications
The drug is in capsule form with each capsule containing 125 or 250 milligrams of oxytetracycline hydrochloride. Oxytetracycline is the antibiotic substance produced by growth of Streptomyces rimosus or the same antibiotic substance produced by any other means.
Dogs
Indication
It is used in dogs for the treatment of bacterial pneumonia caused by Brucella bronchiseptica, tonsillitis caused by Streptococcus hemolyticus, bacterial enteritis caused by Escherichia coli, urinary tract infections caused by Escherichia coli, and wound infections caused by Staphylococcus aureus. The drug can be used for continuation of compatible antibiotic therapy following parenteral oxytetracycline administration where rapidly attained, sustained antibiotic blood levels are required. The duration of treatment required to obtain favorable response will depend to some extent on the severity and degree of involvement and the susceptibility of the infectious agent. Clinical response to antibiotic therapy usually occurs within 48 to 72 hours. If improvement is not observed within that period, the diagnosis and course of treatment should be reconsidered. To assure adequate treatment, administration of the drug should continue for at least 48 hours following favorable clinical response.
Dosage
The drug is administered orally to dogs at a dosage level of 25- 50 milligrams per pound of body weight per day in divided doses at 12-hour intervals.
Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian.
Cats
Indication
It is used in cats for the treatment of bacterial pneumonia caused by Brucella bronchiseptica, tonsillitis caused by Streptococcus hemolyticus, bacterial enteritis caused by Escherichia coli, urinary tract infections caused by Escherichia coli, and wound infections caused by Staphylococcus aureus. The drug can be used for continuation of compatible antibiotic therapy following parenteral oxytetracycline administration where rapidly attained, sustained antibiotic blood levels are required. The duration of treatment required to obtain favorable response will depend to some extent on the severity and degree of involvement and the susceptibility of the infectious agent. Clinical response to antibiotic therapy usually occurs within 48 to 72 hours. If improvement is not observed within that period, the diagnosis and course of treatment should be reconsidered. To assure adequate treatment, administration of the drug should continue for at least 48 hours following favorable clinical response.
Dosage
The drug is administered orally to cats at a dosage level of 25- 50 milligrams per pound of body weight per day in divided doses at 12-hour intervals.
Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian.

FDA page: Open in Animal Drugs @ FDA

Usage

It is used in dogs for the treatment of bacterial pneumonia caused by Brucella bronchiseptica, tonsillitis caused by Streptococcus hemolyticus, bacterial enteritis caused by Escherichia coli, urinary tract infections caused by Escherichia coli, and wound infections caused by Staphylococcus aureus. The drug can be used for continuation of compatible antibiotic therapy following parenteral oxytetracycline administration where rapidly attained, sustained antibiotic blood levels are required. The duration of treatment required to obtain favorable response will depend to some extent on the severity and degree of involvement and the susceptibility of the infectious agent. Clinical response to antibiotic therapy usually occurs within 48 to 72 hours. If improvement is not observed within that period, the diagnosis and course of treatment should be reconsidered. To assure adequate treatment, administration of the drug should continue for at least 48 hours following favorable clinical response. It is used in cats for the treatment of bacterial pneumonia caused by Brucella bronchiseptica, tonsillitis caused by Streptococcus hemolyticus, bacterial enteritis caused by Escherichia coli, urinary tract infections caused by Escherichia coli, and wound infections caused by Staphylococcus aureus. The drug can be used for continuation of compatible antibiotic therapy following parenteral oxytetracycline administration where rapidly attained, sustained antibiotic blood levels are required. The duration of treatment required to obtain favorable response will depend to some extent on the severity and degree of involvement and the susceptibility of the infectious agent. Clinical response to antibiotic therapy usually occurs within 48 to 72 hours. If improvement is not observed within that period, the diagnosis and course of treatment should be reconsidered. To assure adequate treatment, administration of the drug should continue for at least 48 hours following favorable clinical response. Control of infectious synovitis caused by Mycoplasma synoviae susceptible to oxytetracycline.

Source: FDA Animal Drugs @ FDA • Reference

Contraindications

Federal law restricts this drug to use by or on the order of a licensed veterinarian. Prepare a fresh solution daily. Administer 7 to 14 days. Not to be used for more than 14 consecutive days. Use as sole source of drinking water. Do not use in birds producing eggs for human consumption. Prepare a fresh solution daily. Administer up to 14 days. Do not use for more than 14 consecutive days. Use as a sole source of oxytetracycline. Zero-day slaughter withdrawal in swine.

Top Reported Reactions (openFDA)

De-duplicated reaction terms grouped by body system from FDA openFDA reports (not verified; does not prove causation).

Digestive
Vomiting (1) • Cat Decreased appetite (1) • Cat Loss of appetite • Cat

Showing top 5 for Digestive.

Skin & allergy
Hives (1) • Dog

Showing top 5 for Skin & allergy.

Neurologic
Unsteady walking (1) • Cat Tiredness (1) • Cat Head tilt - neurological disorder (1) • Cat

Showing top 5 for Neurologic.

Behavior
Behavioral disorder (1) • Dog

Showing top 5 for Behavior.

Other
Weight loss (1) • Cat Walking difficulty (1) • Cat Urinary bladder disorder NOS (1) • Cat Unsteady gait (1) • Cat Third eyelid extrusion (1) • Cat
Show more (18)
Skin inflammation NOS (1) • Dog Shaking (1) • Dog Partial deafness (1) • Dog Not urinating (1) • Cat Neutrophilia (1) • Dog Nasal discharge (1) • Dog Licking (1) • Dog Leucocytosis NOS (1) • Dog Injection site pain (1) • Dog Head shake - ear disorder (1) • Cat Ear infection NOS (1) • Cat Dilated pupils (1) • Cat Decreased bowel movements (1) • Cat Death by euthanasia (1) • Cat Corneal ulcer (1) • Dog Constipation (1) • Cat Anal sac disorder (1) • Dog Abnormal pupil light reflex (1) • Cat

Showing top 5 for Other.

Data source: FDA openFDA Animal & Veterinary adverse event reports.

Adverse Event Case Summaries (openFDA)

These are individual FDA adverse event reports. They are unverified and do not prove the medication caused the reaction.

No case-level openFDA reports are linked for this medication yet.

Data source: FDA openFDA Animal & Veterinary adverse event reports.

Overdose Information

No approved overdose-management text is linked yet. If overdose is suspected, contact a veterinarian or emergency clinic immediately.

Storage & Handling

No approved storage guidance is linked yet for this ingredient. Use manufacturer packaging and veterinary guidance for handling/storage.

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