Roxee Medication Guide

Doramectin

Medication reference facts with explicit FDA-approval, off-label, source-limited, and safety context. Roxee does not sell, prescribe, or dispense medications.

Both Reference complete FDA data linked Non-Rx Liquid (Solution) Multiple FDA labelers Official label facts Owner quick guide first

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Data freshness

Reference facts

Reference refreshed

Jun 22, 2026, 10:41 a.m.

These are the reference facts Roxee uses on browse cards and quick facts.

FDA applications

FDA application data refreshed

Jun 22, 2026, 10:41 a.m.

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

Safety reports

Safety data refreshed

May 12, 2026, 10:30 a.m.

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

Source timing details

Reference facts: Source Roxee | Refreshed Jun 22, 2026, 10:41 AM UTC
The reference fact projection used for browse cards and quick facts.
Animal Drugs @ FDA: Source FDA | Refreshed Jun 22, 2026, 10:40 AM UTC
Applications/products are imported from FDA export data.
Animal Drugs @ FDA previews: Source FDA | Refreshed Feb 9, 2026, 3:05 AM UTC
Label highlights/doc links are fetched from FDA preview endpoints.
Animal Drug Product Listing Directory (NDC): Source FDA | Refreshed Jun 22, 2026, 10:41 AM UTC
Package/product NDCs from FDA’s electronic listing directory (XLS).
openFDA reaction terms: Source FDA openFDA | Refreshed Jun 22, 2026, 10:45 AM UTC
openFDA case summaries: Source FDA openFDA | Refreshed Jun 22, 2026, 10:45 AM UTC

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Doramectin

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

Both Liquid (Solution) Non-Rx 100% reference complete

Species: Both

Manufacturer: Multiple FDA labelers

Medication Snapshot

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

Doramectin

For the treatment and control of the following nematode and arthropod parasites in swine: Gastrointestinal Roundworms Hyostrongylus rubidus - Adults Ascaris suum - Adults, and fourth-stage larvae Oesophagostomum dentatum - Adults, and fourth-stage larvae Oesophagostomum quadrispinulatum - Adults Strongyloides ransomi - Adults Lungworms Metastrongylus spp. - Adults Kidneyworms Stephanurus dentatus - Adults Sucking Lice Haematopinus suis - Adults and Immature stages Mange Mites Sarcoptes scabiei var. suis - Adults and Immature stages For the treatment and control of the following in cattle: Gastrointestinal roundworms : Ostertagia ostertagi (Adults and fourth-stage larvae) Ostertagia ostertagi (Inhibited fourth-stage larvae) Ostertagia lyrata (Adults and fourth-stage larvae) Haemonchus placei (Adults and fourth-stage larvae) Trichostrongylus axei (Adults and fourth-stage larvae) Trichostrongylus colubriformis (Adults and fourth-stage larvae) Trichostrongylus longispicularis (Adults) Cooperia oncophora (Adults and fourth-stage larvae) Cooperia punctata (Adults and fourth-stage larvae) Cooperia pectinata (Adults) Cooperia surnabada ( syn. mcmasteri ) (Adults and fourth-stage larvae) Bunostomum phlebotomum (Adults) Strongyloides papillosus (Adults) Oesophagostomum radiatum (Adults and fourth-stage larvae) Trichuris spp. (Adults) Lungworms Dictyocaulus viviparus (Adults and fourth-stage larvae) Eyeworms Thelazia spp. (Adults) Grubs Hypoderma bovis Hypoderma lineatum Lice Haematopinus eurysternus Linognathus vituli Solenopotes capillatus Mange mites Psoroptes bovis Sarcoptes scabiei Dectomax injectable solution has been proved to effectively control infections and to protect cattle from reinfection with Cooperia oncophora and Haemonchus placei for 14 days; Ostertagia ostertagi for 21 days; and Cooperia punctata, Oesophagostomum radiatum, and Dictyocaulus viviparus for 28 days after treatment. For treatment and control of gastrointestinal roundworms: Ostertagia ostertagi (adults and fourth- stage larvae), O. ostertagi (inhibited fourth-stage larvae), O. lyrata (adults), Haemonchus placei (adults and fourth-stage larvae), Trichostrongylus axei (adults and fourth-stage larvae), T. colubriformis (adults and fourth-stage larvae), Cooperia oncophora (adults and fourth-stage larvae), C. punctate (adults and fourth-stage larvae), C. pectinate (adults), C. surnabada (adults), Bunostomum phlebotomum (adults), Oesophagostomum radiatum (adults and fourth-stage larvae), Trichuris spp. (adults); lungworms: Dictyocaulus viviparous (adults and fourth-stage larvae); eyeworms: Thelazia gulosa (adults), T. skrjabini (adults); grubs: Hypoderma bovis and H. lineatum ; sucking lice: Linognathus vituli, Haematopinus eurysternus, and Solenopotes capillatus ; biting lice: Damalinia bovis ; mange mites: Chorioptes bovis and Sarcoptes scabiei ; horn flies: Haematobia irritans ; and to control infections and to protect from reinfection with C. oncophora, D. viviparous, O. os Species commonly shown: Both, Beef.

Generic name

Doramectin

Brand names

Dectomax® Injectable Solution for Cattle and Swine, Dectomax® Pour-on Solution for Cattle, DECTOMAX®-CA1, DORACIDE™

Manufacturer

Multiple FDA labelers

Species

Both, Beef, Calves, Dairy

Dosage forms

Liquid (Solution), Injectable Solution, Topical Solution

Prescription

Non-prescription

Completeness

100%

Validation

Complete

Brand names

Dectomax® Injectable Solution for Cattle and Swine Dectomax® Pour-on Solution for Cattle DECTOMAX®-CA1 DORACIDE™ DectoGard™ Doraject™ Doramectin Dectomax Doracide Pour-On Dectomax Pour-On DectoGard Pour-On Doraject Doramectin Pour-On

Dosage forms

Liquid (Solution) Injectable Solution Topical Solution

Indications / Uses

For the treatment and control of the following nematode and arthropod parasites in swine: Gastrointestinal Roundworms Hyostrongylus rubidus - Adults Ascaris suum - Adults, and fourth-stage larvae Oesophagostomum dentatum - Adults, and fourth-stage larvae Oesophagostomum quadrispinulatum - Adults Strongyloides ransomi - Adults Lungworms Metastrongylus spp. - Adults Kidneyworms Stephanurus dentatus - Adults Sucking Lice Haematopinus suis - Adults and Immature stages Mange Mites Sarcoptes scabiei var. suis - Adults and Immature stages For the treatment and control of the following in cattle: Gastrointestinal roundworms : Ostertagia ostertagi (Adults and fourth-stage larvae) Ostertagia ostertagi (Inhibited fourth-stage larvae) Ostertagia lyrata (Adults and fourth-stage larvae) Haemonchus placei (Adults and fourth-stage larvae) Trichostrongylus axei (Adults and fourth-stage larvae) Trichostrongylus colubriformis (Adults and fourth-stage larvae) Trichostrongylus longispicularis (Adults) Cooperia oncophora (Adults and fourth-stage larvae) Cooperia punctata (Adults and fourth-stage larvae) Cooperia pectinata (Adults) Cooperia surnabada ( syn. mcmasteri ) (Adults and fourth-stage larvae) Bunostomum phlebotomum (Adults) Strongyloides papillosus (Adults) Oesophagostomum radiatum (Adults and fourth-stage larvae) Trichuris spp. (Adults) Lungworms Dictyocaulus viviparus (Adults and fourth-stage larvae) Eyeworms Thelazia spp. (Adults) Grubs Hypoderma bovis Hypoderma lineatum Lice Haematopinus eurysternus Linognathus vituli Solenopotes capillatus Mange mites Psoroptes bovis Sarcoptes scabiei Dectomax injectable solution has been proved to effectively control infections and to protect cattle from reinfection with Cooperia oncophora and Haemonchus placei for 14 days; Ostertagia ostertagi for 21 days; and Cooperia punctata , Oesophagostomum radiatum , and Dictyocaulus viviparus for 28 days after treatment. For treatment and control of gastrointestinal roundworms: Ostertagia ostertagi (adults and fourth- stage larvae), O. ostertagi (inhibited fourth-stage larvae), O. lyrata (adults), Haemonchus placei (adults and fourth-stage larvae), Trichostrongylus axei (adults and fourth-stage larvae), T. colubriformis (adults and fourth-stage larvae), Cooperia oncophora (adults and fourth-stage larvae), C. punctate (adults and fourth-stage larvae), C. pectinate (adults), C. surnabada (adults), Bunostomum phlebotomum (adults), Oesophagostomum radiatum (adults and fourth-stage larvae), Trichuris spp. (adults); lungworms: Dictyocaulus viviparous (adults and fourth-stage larvae); eyeworms: Thelazia gulosa (adults), T. skrjabini (adults); grubs: Hypoderma bovis and H. lineatum ; sucking lice: Linognathus vituli , Haematopinus eurysternus , and Solenopotes capillatus ; biting lice: Damalinia bovis ; mange mites: Chorioptes bovis and Sarcoptes scabiei ; horn flies: Haematobia irritans ; and to control infections and to protect from reinfection with C. oncophora , D. viviparous , O. os

Warnings / Contraindications

For use in Cattle and Swine only. This product should not be used in other animal species as severe adverse reactions, including fatalities in dogs, may result.Consult your veterinarian for assistance in the diagnosis, treatment, and control of parasitism. Not for use in female dairy cattle 20 months of age or older. Do not use in calves to be processed for veal. For use in Cattle and Swine only. This product should not be used in other animal species as severe adverse reactions, including fatalities in dogs, may result.Consult your veterinarian for assistance in the diagnosis, treatment, and control of parasitism. Not for use in female dairy cattle 20 months of age or older. Do not use in calves to be processed for veal.

For use in Cattle and Swine only. This product should not be used in other animal species as severe adverse reactions, including fatalities in dogs, may result.Consult your veterinarian for assistance in the diagnosis, treatment, and control of parasitism. Not for use in female dairy cattle 20 months of age or older. Do not use in calves to be processed for veal. For use in Cattle and Swine only. This product should not be used in other animal species as severe adverse reactions, including fatalities in dogs, may result.Consult your veterinarian for assistance in the diagnosis, treatment, and control of parasitism. Not for use in female dairy cattle 20 months of age or older. Do not use in calves to be processed for veal.

Side Effects

Top reported reactions (openFDA): Accidental exposure, Blindness, Death, Labeled drug-species interaction, Lethargy (see also Central nervous system depression in 'Neurological'), Mydriasis.

FAQ

Both, Beef, Calves, excluding veal calves, Dairy, not breeding age, Dairy, females Under 20 months of age

No. Roxee does not currently show this as prescription-only.

Liquid (Solution), Injectable Solution, Topical Solution

Related Conditions

Gastrointestinal (additional) Mange (sarcoptic mange, demodicosis) Myiasis (fly strike) Pica

Source Transparency

Verified source: https://www.roxee.ai/meds/
Verified source: https://animaldrugsatfda.fda.gov
Verified source: https://animaldrugsatfda.fda.gov/adafda/views/#/search
Verified source: https://api.fda.gov/animalandveterinary/event.json
Verified source: https://www.roxee.ai/conditions/
Verified source: https://www.accessdata.fda.gov/spl/data/3daa3695-c74f-414d-b0a9-30d440abbcca/3daa3695-c74f-414d-b0a9-30d440abbcca.xml
Last refreshed: Jun 22, 2026, 10:41 a.m.
Last verified: Feb 12, 2026, 10:44 p.m.
Validation status: Complete

Add to My Pet's Medications

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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 prevention and treatment of infestations caused by larvae of Cochliomyia hominivorax (myiasis), and prevention of reinfestation for 21 days in cattle.

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:

For use in Cattle and Swine only
This product should not be used in other animal species as severe adverse reactions, including fatalities in dogs, may result.Consult your veterinarian for assistance in the diagnosis, treatment, and control of parasitism
Not for use in female dairy cattle 20 months of age or older
Do not use in calves to be processed for veal
Vials, Damaged (1 reports)
Unable to stand (1 reports)
Tremors (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.

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?

Next actions

Talk to a Vet / Find a Vet Near You Save to pet meds Share page Review report evidence

Research brief

Medication Research Insights

A source-aware map of what to know, what is uncertain, and what to verify with your veterinarian.

Source Backed Signals

What to know

Evidence-backed context Limited

Roxee has limited cited overview evidence for Doramectin; use the official documents and your veterinarian's instructions for product-specific decisions.

Source: openFDA case USA-USFDACVM-2023-US-007327

Safety signal coverage Reported signals

28 tracked reaction signals; 27 reported cases; 22 serious reports; 2 species groups. These are reporting and label-derived signals for interpretation with a veterinarian.

Source: openFDA case USA-USFDACVM-2023-US-007327

Interpretation guardrail Not causation

Adverse-event reports help form a watch list, but they do not prove the medication caused the reaction and they are not a risk ranking between medications.

Evidence tension

Stronger signal Label / review

Official labels, package inserts, and reviewed summaries carry more weight than isolated reports.

Source: openFDA case USA-USFDACVM-2023-US-007327

Weaker signal Reported data

Case reports and openFDA terms are useful for pattern awareness, but they are incomplete, can include multiple exposures, and do not estimate an individual pet's probability of harm.

Reaction signal map

Most reported reactions Top terms

Vials, Damaged (1 reports), Unable to stand (1 reports), Tremors (1 reports), Tiredness (lethargy) (1 reports), Shaking (1 reports)

Body systems represented Signal grouping

Digestive (1), Neurologic (4), Effectiveness (2), Other (21)

Explore supporting adverse reports

Species and breed lens

Species represented in reports Species lens

Dog (20 reports), Cat (8 reports)

Breed metadata in reports Metadata only

Beagle (1). These are report metadata, not proof that a breed is at higher risk.

What your vet may verify

Fit for this patient Vet check

Verify whether Doramectin fits the pet's species, current diagnosis, age, weight, organ status, pregnancy/lactation status, and concurrent medications.

Evidence limitations Evidence review

Separate label-backed warnings from adverse-event reports and owner observations before changing the plan.

What to watch next

Watch list Owner-safe

For use in Cattle and Swine only, This product should not be used in other animal species as severe adverse reactions, including fatal, Not for use in female dairy cattle 20 months of age or older, Do not use in calves to be processed for veal, Vials, Damaged

Call sooner if Escalation

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

Bottom line: Use this Doramectin brief as a structured watch list and source map, not as a reason to start, stop, or change treatment without your veterinarian.

Vet source depth

openFDA case USA-USFDACVM-2023-US-007327 · adverse_reaction · adverse reactions
Contraindication source · fda_animal_drugs · warnings contraindications
FDA application profile · official_label · quick facts
FDA application profile · official_label · quick facts
Medication usage source · fda_animal_drugs · quick facts
FOI · document · documents
SPL · document · documents
FOI · document · documents

Evidence

Review status / Updated / Sources

Review status: Clinical reviewer not listed

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

Sources:

FDA application profile · official_label
FDA application profile · official_label
Medication usage source · fda_animal_drugs
Doraject™ · official_label
openFDA case USA-USFDACVM-2023-US-007327 · adverse_reaction

Safety & side effects

Side effects to monitor:

For use in Cattle and Swine only
This product should not be used in other animal species as severe adverse reactions, including fatalities in dogs, may result.Consult your veterinarian for assistance in the diagnosis, treatment, and control of parasitism
Not for use in female dairy cattle 20 months of age or older
Do not use in calves to be processed for veal
Vials, Damaged

Most reported reactions:

Vials, Damaged (1 reports)
Unable to stand (1 reports)
Tremors (1 reports)

Explore reported case details

Emergency warning signs:

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

Talk to a Vet / Find a Vet Near You Start Symptom Intake

Vet Fast Scan

Source-backed clinical checkpoints for quick review.

FDA-labeled species

Beef, Calves, Dairy

Indication / use

For prevention and treatment of infestations caused by larvae of Cochliomyia hominivorax (myiasis), and prevention of reinfestation for 21 days in cattle.

Form / route / dose

Form: Injectable Solution, Liquid (Solution), Topical Solution
Route: Injection, Intramuscular, Subcutaneous, Topical
Confirm product label and patient-specific plan.

Warnings

High: For use in Cattle and Swine only. This product should not be used in other animal species as severe adverse reactions, …

Adverse-event caveat

openFDA adverse-event cases are reported signals. They are not verified, do not prove causation, and do not estimate a pet's individual risk.

Source docs

141-061 Official label / PI
141-061 Official label / PI
141-061 Official label / PI

Quick Facts

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

Species: Both

Manufacturer: Multiple FDA labelers

Form: Injectable Solution, Liquid (Solution), Topical Solution

Identifiers:

ANADA: 200636 ANADA: 200738 ANADA: 200750 NADA: 141061 NADA: 141095 NADA: 141553 NADA: 141616 NDC Package: 20076-0406-1 NDC Package: 20076-0406-2 NDC Package: 20076-2014-9 NDC Package: 30798-315-19 NDC Package: 30798-545-10 NDC Package: 30798-545-13 NDC Package: 30798-545-17 NDC Package: 51072-107-00 NDC Package: 51072-107-01 NDC Package: 51072-107-02 NDC Package: 54771-1685-1 NDC Package: 54771-1685-2 NDC Package: 54771-1685-3

Source metadata:

https://animaldrugsatfda.fda.gov/adafda/views/#/home/previewsearch/141616 · official_label · FDA application profile
https://animaldrugsatfda.fda.gov/adafda/views/#/home/previewsearch/200636 · official_label · FDA application profile
https://animaldrugsatfda.fda.gov · fda_animal_drugs · Medication usage source

Warnings / Contraindications

High: For use in Cattle and Swine only. This product should not be used in other animal species as severe adverse reactions, including fatalities in dogs, may result.Consult your veterinarian for assistance in the diagnosis, treatment, and control of parasitism. Not for use in female dairy cattle 20 months of age or older. Do not use in calves to be processed for veal. For use in Cattle and Swine only. This product should not be used in other animal species as severe adverse reactions, including fatalities in dogs, may result.Consult your veterinarian for assistance in the diagnosis, treatment, and control of parasitism. Not for use in female dairy cattle 20 months of age or older. Do not use in calves to be processed for veal.

Source metadata:

https://animaldrugsatfda.fda.gov · fda_animal_drugs · Contraindication source

Adverse Reactions

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

Reported case explorer

Filter stored openFDA reports by pet and report attributes. Counts describe reports in this data set, not risk.

Clear filters

openFDA adverse-event cases are reported signals. They are not verified, do not prove causation, and do not estimate a pet's individual risk.

Stored reports

Matching reports

Active filters

Selected filters

Reaction: Accidental exposure Clear

Species

Breed

Size / weight

Age

Sex

Seriousness

Outcome

Reaction

Body system

Region

Received after

Received before

Reset

Drill into common report signals

Accidental exposure (1) Administration error NOS (1) Blindness (1) Disorientation (1) Other (1)

Showing up to 50 matching reports.

USA-USFDACVM-2025-US-067187

Received 2025-11-13 · MSK · MSK

Serious

Species: Dog
Breed: Beagle
Size / weight: 25-49 lb (11.34 Kilogram)
Age: 4-7 years (4 Year)
Sex: Female Unknown
Region: USA
Reactions: DisorientationBlindnessShakingAccidental exposureAdministration error NOS
Body systems: Other
Outcomes: Ongoing

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

Tracked signals

Reported cases

Serious reports

Species represented

Grouped by Body System

Digestive (1) · Vomiting Neurologic (4) · Unsteady walking (ataxia), Tremors, Tiredness (lethargy) Effectiveness (2) · Lack of efficacy (endoparasite) - hookworm, Lack of efficacy (endoparasite) - heartworm Other (21) · Vials, Damaged, Unable to stand, Shaking

Most Reported Reactions

Body system	Cases	Species	Serious cases
Other	1	Dog	1
Other	1	Dog	1
Neurologic	1	Cat	1
Neurologic	1	Cat	1
Other	1	Dog	1
Neurologic	1	Cat	1
Other	1	Cat	1
Other	1	Cat	1

Species coverage: Dog (20) Cat (8)

View detailed reaction table

Body system	Species	Seriousness	Frequency	Reports
Digestive	Dog	Non-serious	-	1
Other	Dog	Serious	-	1
Neurologic	Dog	Non-serious	-	1
Other	Dog	Serious	-	1
Neurologic	Cat	Serious	-	1
Neurologic	Cat	Serious	-	1
Other	Dog	Serious	-	1
Neurologic	Cat	Serious	-	1
Other	Cat	Serious	-	1
Other	Dog	Non-serious	-	1
Other	Cat	Serious	-	1
Other	Dog	Non-serious	-	1
Effectiveness	Dog	Non-serious	-	1
Effectiveness	Dog	Serious	-	1
Other	Dog	Serious	-	1
Other	Dog	Serious	-	1
Other	Dog	Serious	-	1
Other	Dog	Serious	-	1
Other	Dog	Serious	-	1
Other	Cat	Serious	-	1
Other	Dog	Serious	-	1
Other	Dog	Serious	-	1
Other	Dog	Serious	-	1
Other	Cat	Serious	-	1
Other	Dog	Serious	-	1
Other	Dog	Serious	-	1
Other	Cat	Serious	-	1
Other	Dog	Unknown	-	-

Source metadata:

https://api.fda.gov/animalandveterinary/event.json · adverse_reaction · openFDA case USA-USFDACVM-2023-US-007327

Source Documents

The most useful source links appear first; full previews and metadata stay in the veterinary/professional layer.

Use original documents to confirm product-specific warnings, ingredients, and handling details with your veterinarian.

141-061 Official label / PI · EA 141-061 Official label / PI · FONSI 141-061 Official label / PI · EA

Full source previews and metadata remain in the veterinary/professional layer.

Owner handouts

No owner handouts linked yet.

Official label / PI

SPL

Open original

DECTOMAX®-CA1

SPL · SPL

Open original

FDA Structured Product Label

DECTOMAX®-CA1

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.
C: 141-616
Status: OTC
Form: Injectable Solution
Route: Injection

Composition / specifications

Each milliliter of solution contains 10 milligrams of doramectin.

Label highlights

Indication

For prevention and treatment of infestations caused by larvae of Cochliomyia hominivorax (myiasis), and prevention of reinfestation for 21 days in cattle.

Dosage

1 mL (10 mg doramectin) per 110 lb of body weight (200 mcg/kg) administered by subcutaneous or intramuscular injection in the neck region.

DORACIDE™

SPL · SPL

Open original

FDA Structured Product Label

DORACIDE™

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 Ltd.
ANADA: 200-636
Status: OTC
Form: Topical Solution
Route: Topical

Composition / specifications

5 mg/mL

Cattle

Indication

DORACIDE™ Pour-On solution is indicated for the treatment and control of the following species of gastrointestinal roundworms, lungworms, eyeworms, grubs, biting and sucking lice, horn flies, and mange mites in cattle.
Gastrointestinal roundworms
Ostertagia ostertagi (adults and L4, including inhibited larvae)
O. lyrata (adults)
Haemonchus placei (adults and L4)
Trichostrongylus axei (adults and L4)
T. colubriformis (adults and L4)
Cooperia oncophora (adults1 and L4)
C. pectinata (adults)
C. punctata (adults and L4)
C. surnabada (adults)
Bunostomum phlebotomum (adults)
Oesophagostomum radiatum (adults and L4)
Trichuris spp. (adults)
1Efficacy below 90% was observed against adult C. oncophora in some clinical studies.

Lungworms (adults and fourth stage larvae)
Dictyocaulus viviparus
Eyeworms
Thelazia gulosa (adults)
T. skrjabini (adults)
Lice
Biting Lice
Bovicola (Damalinia) bovis
Sucking Lice
Haematopinus eurysternus
Linognathus vituli
Solenopotes capillatus
Grubs
Hypoderma bovis
H. lineatum
Horn Flies
Haematobia irritans
Mange Mites
Chorioptes bovis
Sarcoptes scabiei

Doramectin topical solution has been proved to effectively control infections and to protect cattle from reinfection with Cooperia oncophora, Dictyocaulus viviparus, Ostertagia ostertagi, and Oesophagostomum radiatum for 28 days; and Cooperia punctata and Haemonchus placei for 35 days after treatment.

Doramectin topical solution has been proved to effectively control infestations and to protect cattle from reinfestation with Bovicola (Damalinia) bovis for 77 days and Linognathus vituli for 42 days after treatment.

Management Considerations for Horn Flies
DORACIDE™ Pour-On solution provides 7 days of persistent activity against horn flies. The product should be used as part of an integrated control program and be combined with other methods for extended horn fly control.

Dosage

Administer topically at a dosage of 500 mcg doramectin per kg (227 mcg/lb) of body weight. Each mL contains 5 mg of doramectin, sufficient to treat 22 lb (10 kg) of body weight.

Doraject™

SPL · SPL

Open original

FDA Structured Product Label

Doraject™

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.
ANADA: 200-750
Status: OTC
Form: Injectable Solution
Route: Subcutaneous, Intramuscular

Composition / specifications

10 mg/mL

Cattle

Indication

For the treatment and control of the following harmful species of gastrointestinal roundworms, lungworms, eyeworms, grubs, sucking lice, and mange mites.

Gastrointestinal Roundworms (adults and fourth stage larvae)
Ostertagia ostertagi (including inhibited larvae)
O. lyrata
Haemonchus placei
Trichostrongylus axei
T. colubriformis
T. longispicularis1
Cooperia oncophora
C. pectinata1
C. punctata
C. surnabada (syn. mcmasteri)
Bunostomum phlebotomum1
Strongyloides papillosus1
Oesophagostomum radiatum
Trichuris spp.1
Lungworms (adults and fourth stage larvae)
Dictyocaulus viviparus
Eyeworms (adults)
Thelazia spp.
Grubs (parasitic stages)
Hypoderma bovis
H. lineatum
Sucking lice
Haematopinus eurysternus
Linognathus vituli
Solenopotes capillatus
Mange Mites
Psoroptes bovis
Sarcoptes scabiei
1adults
It has been proved to effectively control infections and to protect cattle from reinfection with Cooperia oncophora and Haemonchus placei for 14 days, Ostertagia ostertagi for 21 days, and C. punctata, Oesophagostomum radiatum, and Dictyocaulus viviparus for 28 days after treatment.

Dosage

1 mL (10 mg doramectin) per 110 lb of body weight (200 mcg/kg) administered by subcutaneous (SC) or intramuscular (IM) injection in the neck region.

Swine

Indication

For the treatment and control of the following species of gastrointestinal roundworms, kidney worms, sucking lice, and mange mites.
Gastrointestinal Roundworms
(adults and fourth stage larvae)
Ascaris suum
Oesophagostomum dentatum
Oesophagostomum quadrispinulatum1
Strongyloides ransomi1
Hyostrongylus rubidus1
1adults
Lungworms (adults)
Metastrongylus spp.
Kidney worms (adults)
Stephanurus dentatus
Mange Mites (adults and immature stages)
Sarcoptes scabiei var. suis
Sucking Lice (adults and immature stages)
Haematopinus suis

Dosage

1 mL (10 mg doramectin) per 75 lb of body weight (300 mcg/kg) administered by IM injection only.

Dectomax® Injectable Solution for Cattle and Swine

SPL · SPL

Open original

FDA Structured Product Label

Dectomax® Injectable Solution for Cattle and Swine

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: 141-061
Status: OTC
Form: Liquid (Solution)
Route: Intramuscular, Subcutaneous
Species: Beef • Calves • Dairy

Composition / specifications

Each milliliter of sterile aqueous solution contains 10 milligrams of doramectin.

Swine

Indication

For the treatment and control of the following nematode and arthropod parasites in swine: Gastrointestinal Roundworms Hyostrongylus rubidus - Adults Ascaris suum - Adults, and fourth-stage larvae Oesophagostomum dentatum - Adults, and fourth-stage larvae Oesophagostomum quadrispinulatum - Adults Strongyloides ransomi - Adults Lungworms Metastrongylus spp. - Adults Kidneyworms Stephanurus dentatus - Adults Sucking Lice Haematopinus suis - Adults and Immature stages Mange Mites Sarcoptes scabiei var. suis - Adults and Immature stages

Dosage

300 micrograms per kilogram (10 milligrams per 75 pounds). Administer as a single intramuscular injection.

Limitations

Cattle

Indication

For the treatment and control of the following in cattle: Gastrointestinal roundworms: Ostertagia ostertagi (Adults and fourth-stage larvae) Ostertagia ostertagi (Inhibited fourth-stage larvae) Ostertagia lyrata (Adults and fourth-stage larvae) Haemonchus placei (Adults and fourth-stage larvae) Trichostrongylus axei (Adults and fourth-stage larvae) Trichostrongylus colubriformis (Adults and fourth-stage larvae) Trichostrongylus longispicularis (Adults) Cooperia oncophora (Adults and fourth-stage larvae) Cooperia punctata (Adults and fourth-stage larvae) Cooperia pectinata (Adults) Cooperia surnabada (syn. mcmasteri) (Adults and fourth-stage larvae) Bunostomum phlebotomum (Adults) Strongyloides papillosus (Adults) Oesophagostomum radiatum (Adults and fourth-stage larvae) Trichuris spp. (Adults) Lungworms Dictyocaulus viviparus (Adults and fourth-stage larvae) Eyeworms Thelazia spp. (Adults) Grubs Hypoderma bovis Hypoderma lineatum Lice Haematopinus eurysternus Linognathus vituli Solenopotes capillatus Mange mites Psoroptes bovis Sarcoptes scabiei Dectomax injectable solution has been proved to effectively control infections and to protect cattle from reinfection with Cooperia oncophora and Haemonchus placei for 14 days; Ostertagia ostertagi for 21 days; and Cooperia punctata, Oesophagostomum radiatum, and Dictyocaulus viviparus for 28 days after treatment.

Dosage

200 micrograms per kilogram (10 milligrams per 110 pounds). Administer as a single subcutaneous or intramuscular injection.

Limitations

Not for use in female dairy cattle 20 months of age or older. Do not use in calves to be processed for veal. For use in Cattle and Swine only. This product should not be used in other animal species as severe adverse reactions, including fatalities in dogs, may result.Consult your veterinarian for assistance in the diagnosis, treatment, and control of parasitism.

DectoGard™

SPL · SPL

Open original

FDA Structured Product Label

DectoGard™

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

Sponsor: Aurora Pharmaceutical, Inc.
ANADA: 200-738
Status: OTC
Form: Topical Solution
Route: Topical

Composition / specifications

5 mg/mL

Cattle

Indication

For the treatment and control of the following species of gastrointestinal roundworms, lungworms, eyeworms, grubs, biting and sucking lice, horn flies, and mange mites in cattle.

Gastrointestinal roundworms

Ostertagia ostertagi (adults and L4, including inhibited larvae)
O. lyrata (adults)
Haemonchus placei (adults and L4)
Trichostrongylus axei (adults and L4)
T. colubriformis (adults and L4)
Cooperia oncophora (adults1 and L4)
C. pectinata (adults)
C. punctata (adults and L4)
C. surnabada (adults)
Bunostomum phlebotomum (adults)
Oesophagostomum radiatum (adults and L4)
Trichuris spp. (adults)

1Efficacy below 90% was observed against adult C. oncophora in some clinical studies.

Lungworms (adults and fourth stage larvae)
Dictyocaulus viviparus
Eyeworms
Thelazia gulosa (adults)
T. skrjabini (adults)
Lice
Biting Lice
Bovicola (Damalinia) bovis
Sucking Lice
Haematopinus eurysternus
Linognathus vituli
Solenopotes capillatus
Grubs
Hypoderma bovis
H. lineatum
Horn Flies
Haematobia irritans
Mange Mites
Chorioptes bovis
Sarcoptes scabiei

Doramectin topical solution has been proved to effectively control infections and to protect cattle from reinfection with Cooperia oncophora, Dictyocaulus viviparus, Ostertagia ostertagi, and Oesophagostomum radiatum for 28 days; and Cooperia punctata and Haemonchus placei for 35 days after treatment.

Doramectin topical solution has been proved to effectively control infestations and to protect cattle from reinfestation with Bovicola (Damalinia) bovis for 77 days and Linognathus vituli for 42 days after treatment.

Dosage

Administer topically at a dosage of 500 mcg doramectin per kg (227 mcg/lb) of body weight. Each mL contains 5 mg of doramectin, sufficient to treat 22 lb (10 kg) of body weight.

Dectomax® Pour-on Solution for Cattle

SPL · SPL

Open original

FDA Structured Product Label

Dectomax® Pour-on Solution for Cattle

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: 141-095
Status: OTC
Form: Liquid (Solution)
Route: Topical
Species: Beef • Calves • Dairy

Composition / specifications

Each milliliter of solution contains 5 milligrams of doramectin.

Cattle

Indication

For treatment and control of gastrointestinal roundworms: Ostertagia ostertagi (adults and fourth- stage larvae), O. ostertagi (inhibited fourth-stage larvae), O. lyrata (adults), Haemonchus placei(adults and fourth-stage larvae), Trichostrongylus axei (adults and fourth-stage larvae), T. colubriformis (adults and fourth-stage larvae), Cooperia oncophora (adults and fourth-stage larvae), C. punctate (adults and fourth-stage larvae), C. pectinate (adults), C. surnabada (adults), Bunostomum phlebotomum (adults), Oesophagostomum radiatum (adults and fourth-stage larvae), Trichuris spp. (adults); lungworms: Dictyocaulus viviparous (adults and fourth-stage larvae); eyeworms: Thelazia gulosa (adults), T. skrjabini (adults); grubs: Hypoderma bovis and H. lineatum; sucking lice: Linognathus vituli, Haematopinus eurysternus, and Solenopotes capillatus; biting lice: Damalinia bovis; mange mites: Chorioptes bovis and Sarcoptes scabiei; horn flies: Haematobia irritans; and to control infections and to protect from reinfection with C. oncophora, D. viviparous, O. ostertagi, and O. radiatum for 28 days; and with C. punctate, and H. placei for 35 days after treatment; and to control infestations and to protect from reinfestation with Linognathus vituli for 42 days and with Bovicola (Damalinia) bovis for 77 days after treatment.

Dosage

https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/17486 · document · FOI
https://animaldrugsatfda.fda.gov/adafda/app/search/public/spl/file/17826/DECTOMAX%C2%AE-CA1 · document · SPL
https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/16286 · document · FOI
https://animaldrugsatfda.fda.gov/adafda/app/search/public/spl/file/16625/DORACIDE%E2%84%A2 · document · SPL
https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/14057 · document · FOI
https://animaldrugsatfda.fda.gov/adafda/app/search/public/spl/file/14293/Doraject%E2%84%A2 · document · SPL
https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/594 · document · FOI
https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/593 · document · FOI
https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/3588 · document · FOI
https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/3634 · document · FOI

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

Reference facts: Source Roxee | Refreshed Jun 22, 2026, 10:41 AM UTC
The reference fact projection used for browse cards and quick facts.
Animal Drugs @ FDA: Source FDA | Refreshed Jun 22, 2026, 10:40 AM UTC
Applications/products are imported from FDA export data.
Animal Drugs @ FDA previews: Source FDA | Refreshed Feb 9, 2026, 3:05 AM UTC
Label highlights/doc links are fetched from FDA preview endpoints.
Animal Drug Product Listing Directory (NDC): Source FDA | Refreshed Jun 22, 2026, 10:41 AM UTC
Package/product NDCs from FDA’s electronic listing directory (XLS).
openFDA reaction terms: Source FDA openFDA | Refreshed Jun 22, 2026, 10:45 AM UTC
openFDA case summaries: Source FDA openFDA | Refreshed Jun 22, 2026, 10:45 AM UTC

Official (FDA)

Identity: Generic ingredient • FDA branded products available

Official FDA brands: DectoGard Pour-On Dectomax Dectomax Pour-On Doracide Pour-On Doraject Doramectin Doramectin Pour-On

Manufacturer mapping: Multiple FDA labelers

Case-reported brands (openFDA): MSK

Catalog species: Both • FDA-labeled species: Beef, Calves, Dairy

Rx/OTC: OTC

Form/route: Injectable Solution, Liquid (Solution), Topical Solution • Injection, Intramuscular, Subcutaneous, Topical

Applications: C 141-616 • ANADA 200-636 • ANADA 200-750 • NADA 141-061 • ANADA 200-738 • NADA 141-095

NDC: Packages 20076-0406-1 20076-0406-2 20076-2014-9 30798-315-19 30798-545-10 30798-545-13 • Products 20076 30798 51072 54771 61133 69043

Documents: 20 (FOI: 14) • SPL: 6 • Label highlights • Official documents

Safety (openFDA)

Top reactions: Dog 5 • Cat 0 • View

Case summaries: 1 (showing 1) • View

openFDA reports are unverified and do not prove causation.

Explore

Related conditions: Gastrointestinal (additional) Mange (sarcoptic mange, demodicosis) Myiasis (fly strike) Pica

Linked using: Fda_Label (0.95), Fda_Label (0.95), Fda_Label (0.95)

Diagnosis Codes

Diagnosis-code mappings are not available for this medication yet.

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

For use in Cattle and Swine only. This product should not be used in other animal species as severe adverse reactions, including fatalities in dogs, may result.Consult your veterinarian for assistance in the diagnosis, treatment, and control of parasitism. Not for use in female dairy cattle 20 months of age or older. Do not use in calves to be processed for veal. For use in Cattle and Swine only. This product should not be used in other animal species as severe adverse reactions, including fatalities in dogs, may result.Consult your veterinarian for assistance in the diagnosis, treatment, and control of parasitism. Not for use in female dairy cattle 20 months of age or older. Do not use in calves to be processed for veal. (Contraindication, High)

Top reaction signals

Vials, Damaged (1) Unable to stand (1) Tremors (1) Tiredness (lethargy) (1) Shaking (1) Seizure NOS (1) Respiratory distress (1) Not himself/herself (1)

Identifiers & Packages

Normalized identifiers (NDC/NADA/ANADA) and package metadata from regulator listings.

Identifiers

Package NDC	Product NDC	Status
20076-0406-1	20076	-
20076-0406-2	20076	-
20076-2014-9	20076	-
30798-315-19	30798	-
30798-545-10	30798	-
30798-545-13	30798	-
30798-545-17	30798	-
51072-107-00	51072	-
51072-107-01	51072	-
51072-107-02	51072	-
54771-1685-1	54771	-
54771-1685-2	54771	-
54771-1685-3	54771	-
54771-2718-2	54771	-
54771-2718-3	54771	-
54771-2718-4	54771	-
54771-5438-1	54771	-
54771-5438-2	54771	-
54771-5438-3	54771	-
61133-4004-2	61133	-

Enriched Documents

Documents are tiered by source trust: Official, Clinical, Manufacturer, Marketing.

Doramectin SPL • Structured Product Label • Official
FDA Structured Product Label from the electronic animal drug product listing directory.
Doramectin SPL • Structured Product Label • Official
FDA Structured Product Label from the electronic animal drug product listing directory.
Doraject SPL • Structured Product Label • Official
FDA Structured Product Label from the electronic animal drug product listing directory.
DectoGard Pour-On SPL • Structured Product Label • Official
FDA Structured Product Label from the electronic animal drug product listing directory.
Doramectin SPL • Structured Product Label • Official
FDA Structured Product Label from the electronic animal drug product listing directory.
Dectomax SPL • Structured Product Label • Official
FDA Structured Product Label from the electronic animal drug product listing directory.
Doramectin Pour-On SPL • Structured Product Label • Official
FDA Structured Product Label from the electronic animal drug product listing directory.
Doracide Pour-On SPL • Structured Product Label • Official
FDA Structured Product Label from the electronic animal drug product listing directory.
Dectomax Pour-On SPL • Structured Product Label • Official
FDA Structured Product Label from the electronic animal drug product listing directory.
Doracide Pour-On SPL • Structured Product Label • Official
FDA Structured Product Label from the electronic animal drug product listing directory.
FOI Summary o 141-616 Approved September 30, 2025.pdf • FOI summary • Official • March 13, 2026
FDA FOI summary for application 141616
FOI Summary oN 141-553 Approved September 9, 2022.pdf • FOI summary • Official • March 4, 2025
FDA FOI summary for application 141553
FOI Summary oA 200-636 Approved November 20, 2024.pdf • FOI summary • Official • Dec. 2, 2024
FDA FOI summary for application 200636
FOI Summary oA 200-750 Approved May 25, 2023.pdf • FOI summary • Official • June 1, 2023
FDA FOI summary for application 200750
UCM489435.pdf • FOI summary • Official • April 17, 2023
FDA FOI summary for application 141061
N141061 Supp_7_18_1997_.pdf • FOI summary • Official • April 17, 2023
FDA FOI summary for application 141061
N141061 _Supp_09_18_1997.pdf • FOI summary • Official • April 17, 2023
FDA FOI summary for application 141061
UCM116711.pdf • FOI summary • Official • April 17, 2023
FDA FOI summary for application 141061
ucm116701.pdf • FOI summary • Official • April 17, 2023
FDA FOI summary for application 141061
FOI Summary oA 200-738 Approved January 11, 2023.pdf • FOI summary • Official • Feb. 1, 2023
FDA FOI summary for application 200738
N141095 Orig_9_16_1997.pdf • FOI summary • Official • July 9, 2018
FDA FOI summary for application 141095
ucm117099.pdf • FOI summary • Official • July 9, 2018
FDA FOI summary for application 141095
ucm117101.pdf • FOI summary • Official • July 9, 2018
FDA FOI summary for application 141095
ucm117102.pdf • FOI summary • Official • July 9, 2018
FDA FOI summary for application 141095
ucm117105.pdf • FOI summary • Official • July 9, 2018
FDA FOI summary for application 141095

Data Sources & Change Log

Every non-trivial field is expected to include provenance and update timestamps.

Official 144 Clinical 1 Manufacturer 0 Marketing 0

Current Field Facts

side_effects: Top reported reactions (openFDA): Accidental exposure, Blindness, Death, Labeled drug-species interaction, Lethargy (see also Central nervous system depression… (Clinical, 2026-04-11)
contraindications: For use in Cattle and Swine only. This product should not be used in other animal species as severe adverse reactions, including fatalities in dogs, may result… (Official, 2026-04-12)
contraindications: For use in Cattle and Swine only. This product should not be used in other animal species as severe adverse reactions, including fatalities in dogs, may result… (Official, 2026-04-11)
contraindications: For use in Cattle and Swine only. This product should not be used in other animal species as severe adverse reactions, including fatalities in dogs, may result… (Official, 2026-02-12)
indications: Cattle: For treatment and control of gastrointestinal roundworms, lungworms, eyeworms, grubs, sucking lice, and mange mites. It has been proved to effectively … (Official, 2026-06-22)
indications: Cattle: For treatment and control of gastrointestinal roundworms, lungworms, eyeworms, grubs, sucking lice, and mange mites. It has been proved to effectively … (Official, 2026-06-22)
indications: Cattle: For treatment and control of gastrointestinal roundworms, lungworms, eyeworms, grubs, sucking lice, and mange mites. It has been proved to effectively … (Official, 2026-06-21)
indications: Cattle: For treatment and control of gastrointestinal roundworms, lungworms, eyeworms, grubs, sucking lice, and mange mites. It has been proved to effectively … (Official, 2026-06-20)
indications: Cattle: For treatment and control of gastrointestinal roundworms, lungworms, eyeworms, grubs, sucking lice, and mange mites. It has been proved to effectively … (Official, 2026-06-13)
indications: Cattle: For treatment and control of gastrointestinal roundworms, lungworms, eyeworms, grubs, sucking lice, and mange mites. It has been proved to effectively … (Official, 2026-06-12)
indications: Cattle: For treatment and control of gastrointestinal roundworms, lungworms, eyeworms, grubs, sucking lice, and mange mites. It has been proved to effectively … (Official, 2026-06-12)
indications: Cattle: For treatment and control of gastrointestinal roundworms, lungworms, eyeworms, grubs, sucking lice, and mange mites. It has been proved to effectively … (Official, 2026-06-11)
indications: Cattle: For treatment and control of gastrointestinal roundworms, lungworms, eyeworms, grubs, sucking lice, and mange mites. It has been proved to effectively … (Official, 2026-06-11)
indications: Cattle: For treatment and control of gastrointestinal roundworms, lungworms, eyeworms, grubs, sucking lice, and mange mites. It has been proved to effectively … (Official, 2026-06-10)
indications: Cattle: For treatment and control of gastrointestinal roundworms, lungworms, eyeworms, grubs, sucking lice, and mange mites. It has been proved to effectively … (Official, 2026-06-09)
indications: Cattle: For treatment and control of gastrointestinal roundworms, lungworms, eyeworms, grubs, sucking lice, and mange mites. It has been proved to effectively … (Official, 2026-06-08)
indications: Cattle: For treatment and control of gastrointestinal roundworms, lungworms, eyeworms, grubs, sucking lice, and mange mites. It has been proved to effectively … (Official, 2026-06-07)
indications: Cattle: For treatment and control of gastrointestinal roundworms, lungworms, eyeworms, grubs, sucking lice, and mange mites. It has been proved to effectively … (Official, 2026-06-06)
indications: Cattle: For treatment and control of gastrointestinal roundworms, lungworms, eyeworms, grubs, sucking lice, and mange mites. It has been proved to effectively … (Official, 2026-06-05)
indications: Cattle: For treatment and control of gastrointestinal roundworms, lungworms, eyeworms, grubs, sucking lice, and mange mites. It has been proved to effectively … (Official, 2026-06-04)

Recent Revisions

side_effects updated 2026-04-12 10:05 by etl_backfill • Backfilled from existing medication fields
contraindications updated 2026-04-12 10:05 by etl_backfill • Backfilled from existing medication fields
usage updated 2026-04-12 10:05 by etl_backfill • Backfilled from existing medication fields
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
DECTOMAX®-CA1 OTC Doramectin Injectable Solution • Injection Label highlights Official documents	Zoetis Inc.	C 141-616	Approved	Mar 13, 2026
DORACIDE™ OTC Doramectin Topical Solution • Topical Label highlights Official documents	Bimeda Animal Health Ltd.	ANADA 200-636	Approved	Dec 2, 2024
Doraject™ OTC Doramectin Injectable Solution • Subcutaneous, Intramuscular Label highlights Official documents	Cronus Pharma Specialities India Private Ltd.	ANADA 200-750	Approved	Jun 1, 2023
Dectomax® Injectable Solution for Cattle and Swine OTC Doramectin Liquid (Solution) • Intramuscular, Subcutaneous Label highlights Official documents	Zoetis Inc.	NADA 141-061	Approved	Apr 17, 2023
DectoGard™ OTC Doramectin Topical Solution • Topical Label highlights Official documents	Aurora Pharmaceutical, Inc.	ANADA 200-738	Approved	Feb 1, 2023
Dectomax® Pour-on Solution for Cattle OTC Doramectin Liquid (Solution) • Topical Label highlights Official documents	Zoetis Inc.	NADA 141-095	Approved	Jul 9, 2018

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.

Composition / specifications

Each milliliter of solution contains 10 milligrams of doramectin.

Label highlights

Indication

For prevention and treatment of infestations caused by larvae of Cochliomyia hominivorax (myiasis), and prevention of reinfestation for 21 days in cattle.

Dosage

1 mL (10 mg doramectin) per 110 lb of body weight (200 mcg/kg) administered by subcutaneous or intramuscular injection in the neck region.

Limitations

FDA page: Open in Animal Drugs @ FDA

Composition / specifications

5 mg/mL

Cattle

Indication

Dosage

Administer topically at a dosage of 500 mcg doramectin per kg (227 mcg/lb) of body weight. Each mL contains 5 mg of doramectin, sufficient to treat 22 lb (10 kg) of body weight.

Limitations

FDA page: Open in Animal Drugs @ FDA

Composition / specifications

10 mg/mL

Cattle

Indication

Dosage

1 mL (10 mg doramectin) per 110 lb of body weight (200 mcg/kg) administered by subcutaneous (SC) or intramuscular (IM) injection in the neck region.

Limitations

Swine

Indication

Dosage

1 mL (10 mg doramectin) per 75 lb of body weight (300 mcg/kg) administered by IM injection only.

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: Beef • Calves • Dairy

Composition / specifications

Each milliliter of sterile aqueous solution contains 10 milligrams of doramectin.

Swine

Indication

Dosage

300 micrograms per kilogram (10 milligrams per 75 pounds). Administer as a single intramuscular injection.

Limitations

Cattle

Indication

Dosage

200 micrograms per kilogram (10 milligrams per 110 pounds). Administer as a single subcutaneous or intramuscular injection.

Limitations

FDA page: Open in Animal Drugs @ FDA

Composition / specifications

5 mg/mL

Cattle

Indication

For the treatment and control of the following species of gastrointestinal roundworms, lungworms, eyeworms, grubs, biting and sucking lice, horn flies, and mange mites in cattle.

Gastrointestinal roundworms

Ostertagia ostertagi (adults and L4, including inhibited larvae)
O. lyrata (adults)
Haemonchus placei (adults and L4)
Trichostrongylus axei (adults and L4)
T. colubriformis (adults and L4)
Cooperia oncophora (adults1 and L4)
C. pectinata (adults)
C. punctata (adults and L4)
C. surnabada (adults)
Bunostomum phlebotomum (adults)
Oesophagostomum radiatum (adults and L4)
Trichuris spp. (adults)

1Efficacy below 90% was observed against adult C. oncophora in some clinical studies.

Dosage

Administer topically at a dosage of 500 mcg doramectin per kg (227 mcg/lb) of body weight. Each mL contains 5 mg of doramectin, sufficient to treat 22 lb (10 kg) of body weight.

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: Beef • Calves • Dairy

Composition / specifications

Each milliliter of solution contains 5 milligrams of doramectin.

Cattle

Indication

Dosage

5 milligrams per 10 kilograms (5 milligrams per 22 pounds).

Limitations

Not for use in female dairy cattle 20 months of age or older. Do not use in calves to be processed for veal.

FDA page: Open in Animal Drugs @ FDA

Usage

For the treatment and control of the following nematode and arthropod parasites in swine: Gastrointestinal Roundworms Hyostrongylus rubidus - Adults Ascaris suum - Adults, and fourth-stage larvae Oesophagostomum dentatum - Adults, and fourth-stage larvae Oesophagostomum quadrispinulatum - Adults Strongyloides ransomi - Adults Lungworms Metastrongylus spp. - Adults Kidneyworms Stephanurus dentatus - Adults Sucking Lice Haematopinus suis - Adults and Immature stages Mange Mites Sarcoptes scabiei var. suis - Adults and Immature stages For the treatment and control of the following in cattle: Gastrointestinal roundworms : Ostertagia ostertagi (Adults and fourth-stage larvae) Ostertagia ostertagi (Inhibited fourth-stage larvae) Ostertagia lyrata (Adults and fourth-stage larvae) Haemonchus placei (Adults and fourth-stage larvae) Trichostrongylus axei (Adults and fourth-stage larvae) Trichostrongylus colubriformis (Adults and fourth-stage larvae) Trichostrongylus longispicularis (Adults) Cooperia oncophora (Adults and fourth-stage larvae) Cooperia punctata (Adults and fourth-stage larvae) Cooperia pectinata (Adults) Cooperia surnabada ( syn. mcmasteri ) (Adults and fourth-stage larvae) Bunostomum phlebotomum (Adults) Strongyloides papillosus (Adults) Oesophagostomum radiatum (Adults and fourth-stage larvae) Trichuris spp. (Adults) Lungworms Dictyocaulus viviparus (Adults and fourth-stage larvae) Eyeworms Thelazia spp. (Adults) Grubs Hypoderma bovis Hypoderma lineatum Lice Haematopinus eurysternus Linognathus vituli Solenopotes capillatus Mange mites Psoroptes bovis Sarcoptes scabiei Dectomax injectable solution has been proved to effectively control infections and to protect cattle from reinfection with Cooperia oncophora and Haemonchus placei for 14 days; Ostertagia ostertagi for 21 days; and Cooperia punctata , Oesophagostomum radiatum , and Dictyocaulus viviparus for 28 days after treatment. For treatment and control of gastrointestinal roundworms: Ostertagia ostertagi (adults and fourth- stage larvae), O. ostertagi (inhibited fourth-stage larvae), O. lyrata (adults), Haemonchus placei (adults and fourth-stage larvae), Trichostrongylus axei (adults and fourth-stage larvae), T. colubriformis (adults and fourth-stage larvae), Cooperia oncophora (adults and fourth-stage larvae), C. punctate (adults and fourth-stage larvae), C. pectinate (adults), C. surnabada (adults), Bunostomum phlebotomum (adults), Oesophagostomum radiatum (adults and fourth-stage larvae), Trichuris spp. (adults); lungworms: Dictyocaulus viviparous (adults and fourth-stage larvae); eyeworms: Thelazia gulosa (adults), T. skrjabini (adults); grubs: Hypoderma bovis and H. lineatum ; sucking lice: Linognathus vituli , Haematopinus eurysternus , and Solenopotes capillatus ; biting lice: Damalinia bovis ; mange mites: Chorioptes bovis and Sarcoptes scabiei ; horn flies: Haematobia irritans ; and to control infections and to protect from reinfection with C. oncophora , D. viviparous , O. os

Source: FDA Animal Drugs @ FDA • Reference

Contraindications

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) • Dog

Showing top 5 for Digestive.

Neurologic

Unsteady walking (1) • Dog Tremors (1) • Cat Tiredness (1) • Cat Seizure NOS (1) • Cat

Showing top 5 for Neurologic.

Effectiveness

Lack of efficacy (endoparasite) - hookworm (1) • Dog Lack of efficacy (endoparasite) - heartworm (1) • Dog

Showing top 5 for Effectiveness.

Other

Vials, Damaged (1) • Dog Unable to stand (1) • Dog Shaking (1) • Dog Respiratory distress (1) • Cat Panting (1) • Dog

Show more (16)

Not himself/herself (1) • Cat Mydriasis (1) • Dog Labeled drug-species interaction (1) • Dog Intentional misuse (1) • Dog Increased sensitivity to light (1) • Dog Incorrect route of drug administration (1) • Dog Inappropriate packaging or design (1) • Dog Hyperaesthesia (1) • Cat General illness (1) • Dog Disorientation (1) • Dog Dilated pupils (1) • Dog Breathing difficulty (1) • Cat Blindness (1) • Dog Administration error NOS (1) • Dog Accidental exposure (1) • Cat Death • Dog

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.

Dog, Beagle, Female, 4 year, 11.34 kilogram • Drug: MSK, Suspension, Oral • Reactions: Disorientation, Blindness, Shaking, Accidental exposure, Administration error NOS • Outcome: Ongoing

Report ID: USA-USFDACVM-2025-US-067187
Serious AE: Yes
Treated For AE: Yes
Sex: Female
Age: 4.00 Year
Weight: 11.340 Kilogram

Case-reported brand: MSK
Case-reported manufacturer: MSK
Route: Oral
Form: Suspension

Reactions Reported:

Disorientation Blindness Shaking Accidental exposure Administration error NOS

Outcomes: Ongoing

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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Medical Disclaimer: The medication details provided on Roxee are for informational purposes only and are not a substitute for professional veterinary advice. Always consult your veterinarian about your pet's specific needs.

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USA-USFDACVM-2025-US-067187

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