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Roxee Medication Guide

Clindamycin

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 Rx required Capsule Multiple FDA labelers Official label facts Owner quick guide first

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Data freshness

Reference facts
Reference refreshed
Aug 6, 2026, 7:47 p.m.

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

FDA applications
FDA application data refreshed
Aug 6, 2026, 7:47 p.m.

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

Safety reports
Safety data refreshed
Aug 6, 2026, 7:49 p.m.

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

Source timing details
Source timing details
  • Reference facts: Source Roxee | Refreshed Aug 6, 2026, 7:47 PM UTC
    The reference fact projection used for browse cards and quick facts.
  • Animal Drugs @ FDA: Source FDA | Refreshed Aug 6, 2026, 7:47 PM 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 Aug 6, 2026, 7:47 PM UTC
    Package/product NDCs from FDA’s electronic listing directory (XLS).
  • openFDA reaction terms: Source FDA openFDA | Refreshed Aug 6, 2026, 7:52 PM UTC
  • openFDA case summaries: Source FDA openFDA | Refreshed Aug 6, 2026, 7:52 PM UTC
Illustration placeholder
Clindamycin

Clindamycin

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

Both Capsule Rx required 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.

Clindamycin

For the treatment of skin infections (wounds and abscesses) due to susceptible strains of coagulase-positive staphylococci ( Staphylococcus aureus or S. intermedius ), deep wounds and abscesses due to susceptible strains of Bacteroides fragilis, Prevotella melaninogenicus, Fusobacterium necrophorum, and Clostridium perfringens, dental infections due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens, and osteomyelitis due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens . For the treatment of skin infections (wounds and abscesses) due to susceptible strains of coagulase-positive staphylococci ( Staphylococcus aureus or S. intermedius ), deep wounds and abscesses due to susceptible strains of Bacteroides fragilis, Prevotella melaninogenicus, Fusobacterium necrophorum, and Clostridium perfringens, dental infections due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens, and osteomyelitis due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens . For the treatment of skin infections (wounds and abscesses) due to susceptible strains of S. aureus, S. intermedius, Streptococcus species, deep wounds and abscesses due to susceptible strains of Clostridium perfringens and Bacteroides fragilis, and dental infections due to susceptible strains of S. aureus, S. intermedius, Streptococcus species, C. perfringens, and B. fragilis . Species commonly shown: Both, Dog, Cat.

Generic name
Clindamycin
Brand names
Antirobe® Capsules, Antirobe Aquadrops®, Clindamycin Hydrochloride Oral Liquid, Clinsol®
Manufacturer
Multiple FDA labelers
Species
Both, Dog, Cat
Dosage forms
Capsule, Liquid (Solution), Tablet, Liquid
Prescription
Prescription required
Completeness
100%
Validation
Complete
Brand names
Antirobe® Capsules Antirobe Aquadrops® Clindamycin Hydrochloride Oral Liquid Clinsol® Clindamycin Hydrochloride Capsules Clintabs® ClindaRobe™ Clindamycin Hydrochloride Oral Drops ClindaMed™ Oral Drops Clindamycin Hydrochloride Tablets Clindamycin Clindamycin Hydrochloride CLINTABS Antirobe Aquadrops Antirobe ZydaClin
Dosage forms
Capsule Liquid (Solution) Tablet Liquid

Indications / Uses

For the treatment of skin infections (wounds and abscesses) due to susceptible strains of coagulase-positive staphylococci ( Staphylococcus aureus or S. intermedius ), deep wounds and abscesses due to susceptible strains of Bacteroides fragilis , Prevotella melaninogenicus , Fusobacterium necrophorum , and Clostridium perfringens , dental infections due to susceptible strains of S. aureus , B. fragilis , P. melaninogenicus , F. necrophorum , and C. perfringens , and osteomyelitis due to susceptible strains of S. aureus , B. fragilis , P. melaninogenicus , F. necrophorum , and C. perfringens . For the treatment of skin infections (wounds and abscesses) due to susceptible strains of coagulase-positive staphylococci ( Staphylococcus aureus or S. intermedius ), deep wounds and abscesses due to susceptible strains of Bacteroides fragilis , Prevotella melaninogenicus, Fusobacterium necrophorum , and Clostridium perfringens , dental infections due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens , and osteomyelitis due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum , and C. perfringens . For the treatment of skin infections (wounds and abscesses) due to susceptible strains of S. aureus, S. intermedius, Streptococcus species, deep wounds and abscesses due to susceptible strains of Clostridium perfringens and Bacteroides fragilis , and dental infections due to susceptible strains of S. aureus, S. intermedius, Streptococcus species, C. perfringens , and B. fragilis .

Warnings / Contraindications

Federal law restricts this drug to use by or on the order of a licensed veterinarian. Federal law restricts this drug to use by or on the order of a licensed veterinarian

  • Federal law restricts this drug to use by or on the order of a licensed veterinarian. Federal law restricts this drug to use by or on the order of a licensed veterinarian

Side Effects

Top reported reactions (openFDA): Vomiting, Death by euthanasia, Lethargy (see also Central nervous system depression in 'Neurological'), Anorexia, Other abnormal test result NOS, Lack of efficacy - NOS.

FAQ

Both, Dog, Cat

Yes. Roxee shows this as prescription-only.

Capsule, Liquid (Solution), Tablet, Liquid

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 the treatment of skin infections (wounds and abscesses) due to susceptible strains of coagulase-positive staphylococci ( Staphylococcus aureus or S. intermedius ), deep wounds and abscesses due to susceptible strains...

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:

  • Loss of appetite (1 reports)
  • Diarrhea (1 reports)
  • Dermal thickening (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?

Next actions

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 Clindamycin; use the official documents and your veterinarian's instructions for product-specific decisions.

Source: openFDA case USA-USFDACVM-2026-US-013066
Safety signal coverage Reported signals

32 tracked reaction signals; 32 reported cases; 24 serious reports; 2 species groups. These are reporting and label-derived signals for interpretation with a veterinarian.

Source: openFDA case USA-USFDACVM-2026-US-013066
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-2026-US-013066
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

Loss of appetite (1 reports), Diarrhea (1 reports), Dermal thickening (1 reports), Dehydration (1 reports), Decreased cholesterol (1 reports)

Body systems represented Signal grouping

Digestive (3), Skin & allergy (1), Neurologic (2), Behavior (1)

Explore supporting adverse reports

Species and breed lens

Species represented in reports Species lens

Dog (27 reports), Cat (5 reports)

Breed metadata in reports Metadata only

Domestic Shorthair (5), Schnauzer - Miniature (2), Samoyed (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 Clindamycin 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

Loss of appetite, Diarrhea, Dermal thickening

Call sooner if Escalation

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

Bottom line: Use this Clindamycin 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
  1. openFDA case USA-USFDACVM-2026-US-013066 · adverse_reaction · adverse reactions
  2. Contraindication source · fda_animal_drugs · warnings contraindications
  3. FDA application profile · official_label · quick facts
  4. FDA application profile · official_label · quick facts
  5. Medication usage source · fda_animal_drugs · quick facts
  6. FOI · document · documents
  7. SPL · document · documents
  8. FOI · document · documents

Evidence

Review status / Updated / Sources

Review status: Clinical reviewer not listed

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

Sources:
Safety & side effects

Side effects to monitor:

  • Loss of appetite
  • Diarrhea
  • Dermal thickening

Most reported reactions:

  • Loss of appetite (1 reports)
  • Diarrhea (1 reports)
  • Dermal thickening (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.

Vet Fast Scan

Source-backed clinical checkpoints for quick review.

FDA-labeled species
Cat, Dog
Indication / use
For the treatment of skin infections (wounds and abscesses) due to susceptible strains of coagulase-positive staphylococci ( Staphylococcus aureus or S. intermedius ), deep wounds…
Form / route / dose
Form: Capsule, Liquid, Liquid (Solution), Tablet
Route: Oral
Confirm product label and patient-specific plan.
Warnings
  • High: Federal law restricts this drug to use by or on the order of a licensed veterinarian. Federal law restricts this drug t…
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.

Quick Facts

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

Species: Both
Manufacturer: Multiple FDA labelers
Form: Capsule, Liquid, Liquid (Solution), Tablet
Identifiers:
ANADA: 200193 ANADA: 200291 ANADA: 200298 ANADA: 200316 ANADA: 200383 ANADA: 200398 ANADA: 200538 ANADA: 200813 NADA: 120161 NADA: 135940 NDC Package: 13985-957-25 NDC Package: 51311-400-40 NDC Package: 51311-402-75 NDC Package: 51311-404-15 NDC Package: 54771-3043-1 NDC Package: 54771-3044-1 NDC Package: 54771-3045-1 NDC Package: 54771-3179-1 NDC Package: 54771-3179-2 NDC Package: 69043-013-20
Source metadata:

Warnings / Contraindications

Federal law restricts this drug to use by or on the order of a licensed veterinarian. Federal law restricts this drug to use by or on the order of a licensed veterinarian

  • High: Federal law restricts this drug to use by or on the order of a licensed veterinarian. Federal law restricts this drug to use by or on the order of a licensed veterinarian
Source metadata:

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
21
Matching reports
21
Active filters
0
Reset
Showing up to 50 matching reports.

USA-USFDACVM-2026-US-014603

Received 2026-03-18 · MSK · MSK

Non-serious
Species
Dog
Breed
Schnauzer - Miniature
Size / weight
10-24 lb (7.212 Kilogram)
Age
8+ years (14 Year)
Sex
Male Neutered
Region
USA
Reactions
AtaxiaCollapse of legElevated blood urea nitrogen (BUN)Elevated cholesterol (total)WeaknessConfusionHyperphosphataemiaElevated symmetrical dimethylarginine (SDMA)Hind limb ataxiaDifficulty standingDifficulty going up/down stairsCircling - neurological disorder (see also Behavioural disorders)
Body systems
NeurologicOther
Outcomes
Ongoing

USA-USFDACVM-2026-US-014257

Received 2026-03-17 · MSK · MSK

Serious
Species
Cat
Breed
Domestic Shorthair
Size / weight
Under 10 lb (4.53 Kilogram)
Age
1-3 years (2 Year)
Sex
Female Neutered
Region
USA
Reactions
Limb amputationInjection site sarcomaBehavioural disorder NOSLethargy (see also Central nervous system depression in Neurological)Localised pain NOS (see other SOCs for specific pain)VocalisationLimpingInjection site mass NOS
Body systems
OtherBehaviorNeurologic
Outcomes
Outcome Unknown

USA-USFDACVM-2026-US-014092

Received 2026-03-16 · MSK · MSK

Serious
Species
Cat
Breed
Domestic Shorthair
Size / weight
Under 10 lb (4.354 Kilogram)
Age
4-7 years (7 Year)
Sex
Female Neutered
Region
USA
Reactions
DroolingReluctant to moveNot eatingDilated pupilsNot himself/herselfHypothermiaTachypnoeaIntentional misuseLeukopenia NOSHypoglycaemiaElevated symmetrical dimethylarginine (SDMA)AzotaemiaLow ionized calcium (Ca; Hypocalcaemia, ionized)ObtundedWeak pulseLateral recumbencyRegurgitationCardiac arrestDeath
Body systems
DigestiveOther
Outcomes
Died

USA-USFDACVM-2026-US-013313

Received 2026-03-16 · MSK · MSK

Serious
Species
Cat
Breed
Domestic Shorthair
Size / weight
10-24 lb (6.427 Kilogram)
Age
8+ years (13 Year)
Sex
Female Neutered
Region
USA
Reactions
PruritusSkin lesion NOSSkin scab
Body systems
Skin & allergyOther
Outcomes
Ongoing

USA-USFDACVM-2026-US-013066

Received 2026-03-16 · MSK · MSK

Serious
Species
Dog
Breed
Samoyed
Size / weight
50-99 lb (24.948 Kilogram)
Age
8+ years (9 Year)
Sex
Male Neutered
Region
USA
Reactions
Lethargy (see also Central nervous system depression in Neurological)ShakingPale mucous membraneCold feeling of extremityVomitingTachycardiaLaboured breathingTachypnoeaDehydrationWeak pulseTense abdomenHypochloraemiaHyponatremiaAzotaemiaHypocalcaemiaHypoglycaemiaHyperphosphataemiaHypoproteinaemiaHypoalbuminaemiaLow alanine aminotransferase (ALT)Elevated lactateIncreased percentage reticulocytesLymphocytosisMonocytosisAbnormal red blood cellHypotensionAbdominal effusionAspiration pneumoniaHeart murmurGastric perforationLateral recumbencySepticaemiaCoagulopathyHypernatraemiaHypercalcaemiaElevated serum alkaline phosphatase (ALP)NeutrophiliaStridor (Upper respiratory; for lower respiratory see also Bronchial rale)Unresponsive to stimuliCyanotic mucous membranesThrombosisOedema of the extremities (see also other SOCs for most applicable oedema)Pitting oedemaLamenessElevated aspartate aminotransferase (AST)Stertor
Body systems
NeurologicOtherDigestive
Outcomes
Ongoing

USA-USFDACVM-2026-US-012493

Received 2026-03-16 · MSK · MSK

Non-serious
Species
Dog
Breed
Schnauzer - Miniature
Size / weight
10-24 lb (7.212 Kilogram)
Age
8+ years (14 Year)
Sex
Male Neutered
Region
USA
Reactions
AtaxiaCollapse of legElevated blood urea nitrogen (BUN)Elevated cholesterol (total)WeaknessConfusionHyperphosphataemiaElevated symmetrical dimethylarginine (SDMA)
Body systems
NeurologicOther
Outcomes
Ongoing

USA-USFDACVM-2026-US-010698

Received 2026-02-24 · MSK · MSK

Non-serious
Species
Cat
Breed
Domestic Shorthair
Size / weight
10-24 lb (6.427 Kilogram)
Age
8+ years (13 Year)
Sex
Female Neutered
Region
USA
Reactions
PruritusSkin lesion NOSSkin scabLabeled drug-species interactionIntentional misuse
Body systems
Skin & allergyOther
Outcomes
Ongoing

USA-USFDACVM-2026-US-007430

Received 2026-02-19 · MSK · MSK

Non-serious
Species
Cat
Breed
Domestic Shorthair
Size / weight
10-24 lb (4.98 Kilogram)
Age
8+ years (8 Year)
Sex
Female Neutered
Region
USA
Reactions
Dilated pupilsHyperactivityQuiet
Body systems
Other
Outcomes
Ongoing

USA-USFDACVM-2026-US-007170

Received 2026-02-17 · MSK · MSK

Non-serious
Species
Cat
Breed
Domestic Shorthair
Size / weight
10-24 lb (5.57 Kilogram)
Age
8+ years (9 Year)
Sex
Male Neutered
Region
USA
Reactions
VomitingWeaknessNot eatingLimb weaknessElevated betahydroxybutyrate (BHBA)Excessive appetiteHyperglycaemia
Body systems
DigestiveOther
Outcomes
Ongoing

USA-USFDACVM-2026-US-005573

Received 2026-01-30 · MSK · MSK

Non-serious
Species
Dog
Breed
['Retriever - Labrador', 'Chow Chow']
Size / weight
50-99 lb (24.95 Kilogram)
Age
4-7 years (5 Year)
Sex
Female Neutered
Region
USA
Reactions
Localised oedema (not application site)WoundSwollen limbLickingLocalised pain NOS (see other SOCs for specific pain)Tooth disorder
Body systems
Other
Outcomes
Ongoing

USA-USFDACVM-2026-US-003714

Received 2026-01-29 · MSK · MSK

Non-serious
Species
Dog
Breed
Schnauzer - Miniature
Size / weight
10-24 lb (7.212 Kilogram)
Age
8+ years (14 Year)
Sex
Male Neutered
Region
USA
Reactions
AtaxiaCollapse of legElevated blood urea nitrogen (BUN)Elevated cholesterol (total)WeaknessConfusionHyperphosphataemiaElevated symmetrical dimethylarginine (SDMA)Discomfort NOS
Body systems
NeurologicOther
Outcomes
Ongoing

USA-USFDACVM-2025-US-074897

Received 2025-12-12 · MSK · MSK

Serious
Species
Dog
Breed
['Chihuahua', 'Dog (unknown)']
Size / weight
Under 10 lb (2.26 Kilogram)
Age
Under 1 year (2 Week)
Sex
Female Intact
Region
USA
Reactions
IcterusDeathOther abnormal test result NOSElevated liver enzymes NOSSwollen jointLocalised hair lossSkin lesion NOSConjunctival oedemaCorneal oedemaSkin scabSwollen limbLethargy (see also Central nervous system depression in Neurological)AnorexiaEar infection NOSLocal swelling (not application site)
Body systems
OtherSkin & allergyNeurologicDigestive
Outcomes
Died

USA-USFDACVM-2025-US-071574

Received 2025-12-05 · MSK · MSK

Serious
Species
Dog
Breed
Spitz - German Pomeranian
Size / weight
Under 10 lb (1.633 Kilogram)
Age
4-7 years (4 Year)
Sex
Female Neutered
Region
USA
Reactions
Decreased appetiteVomiting bileDiarrhoeaElectrolyte disorderHypoalbuminaemiaDecreased cholesterol (total)Low creatinineWeight loss
Body systems
DigestiveOther
Outcomes
Ongoing

USA-USFDACVM-2025-US-071565

Received 2025-12-03 · MSK · MSK

Serious
Species
Dog
Breed
Dog (unknown)
Size / weight
25-49 lb (14.969 Kilogram)
Age
8+ years (15 Year)
Sex
Male Neutered
Region
USA
Reactions
Head tilt - neurological disorder (see also Head tilt - ear disorder)Walking difficultyVomitingSkin and tissue infection NOSGeneral illnessDeath
Body systems
NeurologicOtherDigestive
Outcomes
Died

USA-USFDACVM-2025-US-072712

Received 2025-12-01 · MSK · MSK

Non-serious
Species
Cat
Breed
Domestic Shorthair
Size / weight
Under 10 lb (3.175 Kilogram)
Age
8+ years (15 Year)
Sex
Female Neutered
Region
USA
Reactions
Not eatingHead tilt - ear disorderElevated blood urea nitrogen (BUN)
Body systems
Other
Outcomes
Ongoing

USA-USFDACVM-2025-US-074320

Received 2025-11-24 · MSK · MSK

Serious
Species
Dog
Breed
['Terrier (unspecified)', 'Dog (unknown)']
Size / weight
25-49 lb (18.14 Kilogram)
Age
8+ years (9 Year)
Sex
Male Neutered
Region
USA
Reactions
Behavioural disorder NOSEpidermal collaretteHepatic toxicosisDermal thickeningPyodermaJoint swellingLocal swelling (not application site)Skin ulcerLethargy (see also Central nervous system depression in Neurological)ItchingHair loss NOSDeathInappetence
Body systems
BehaviorOtherSkin & allergyNeurologic
Outcomes
Died

USA-USFDACVM-2025-US-070095

Received 2025-11-22 · MSK · MSK

Serious
Species
Dog
Breed
Terrier - Boston
Size / weight
25-49 lb (12.247 Kilogram)
Age
8+ years (11 Year)
Sex
Male Neutered
Region
USA
Reactions
Ear irritationPolypEye inflammation NOSEye irritationAbnormal cytologyScratchingMedication error NOSEar painEar canal inflammationCorneal disorder NOSCorneal oedemaCorneal ulcerIncreased intra-ocular pressure
Body systems
Other
Outcomes
Ongoing

USA-USFDACVM-2025-US-073374

Received 2025-11-17 · MSK · MSK

Serious
Species
Cat
Sex
Male Unknown
Region
USA
Reactions
Neurological symptoms NOS
Body systems
Neurologic
Outcomes
Euthanized

USA-USFDACVM-2025-US-068424

Received 2025-11-17 · MSK · MSK

Serious
Species
Dog
Breed
['Terrier (unspecified)', 'Dog (unknown)']
Size / weight
25-49 lb (18.14 Kilogram)
Age
8+ years (9 Year)
Sex
Male Neutered
Region
USA
Reactions
Behavioural disorder NOSEpidermal collaretteHepatic toxicosisDermal thickeningPyodermaJoint swellingLocal swelling (not application site)Skin ulcerLethargy (see also Central nervous system depression in Neurological)ItchingHair loss NOSDeathInappetence
Body systems
BehaviorOtherSkin & allergyNeurologic
Outcomes
Died

USA-USFDACVM-2025-US-065825

Received 2025-11-05 · MSK · MSK

Serious
Species
Cat
Breed
Domestic Mediumhair
Size / weight
Under 10 lb (3.719 Kilogram)
Age
8+ years (12 Year)
Sex
Male Neutered
Region
USA
Reactions
Reluctant to moveWobblinessNasal congestionSleepiness - systemic disorderHind limb paralysisThrombosisParalysisDeath by euthanasia
Body systems
Other
Outcomes
Euthanized

USA-USFDACVM-2025-US-063054

Received 2025-10-16 · MSK · MSK

Non-serious
Species
Cat
Breed
Domestic Shorthair
Size / weight
Under 10 lb (2.54 Kilogram)
Age
8+ years (1 Year)
Sex
Female Unknown
Region
USA
Reactions
Lack of efficacy - NOSNon-regenerative anaemia
Body systems
EffectivenessOther
Outcomes
Ongoing

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

Tracked signals
32
Reported cases
32
Serious reports
24
Species represented
2
Grouped by Body System
Digestive (3) · Loss of appetite, Diarrhea, Decreased appetite Skin & allergy (1) · Application site hair loss Neurologic (2) · Unsteady walking (ataxia), Circling - neurological disorder Behavior (1) · Behavioral disorder (unspecified) Other (25) · Difficulty standing, Difficulty going up/down stairs, Dermal thickening
Most Reported Reactions
Reaction Body system Cases Species Serious cases
Digestive 1 Dog 1
Digestive 1 Dog 1
Other 1 Dog 1
Other 1 Dog 1
Other 1 Dog 1
Digestive 1 Dog 1
Other 1 Cat 1
Other 1 Dog 1

Species coverage: Dog (27) Cat (5)

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

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.

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

Owner handouts

0
No owner handouts linked yet.

Official label / PI

0
No official label or package insert links yet.

SPL

17

FOI

15

Clindamycin Hydrochloride Tablets

SPL · SPL

FDA Structured Product Label

Clindamycin Hydrochloride 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
Felix Pharmaceuticals Pvt. Ltd.
ANADA
200-813
Status
RX
Form
Tablet
Route
Oral
Composition / specifications
25 mg, 75 mg, and 150 mg

Dogs

Indication

For the treatment of skin infections (wounds and abscesses) due to susceptible strains of coagulase-positive staphylococci (Staphylococcus aureus or S. intermedius), deep wounds and abscesses due to susceptible strains of Bacteroides fragilis, Prevotella melaninogenicus, Fusobacterium necrophorum, and Clostridium perfringens, dental infections due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens, and osteomyelitis due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens.

Dosage

Wounds, abscesses, and dental infections: 2.5 to 15 mg per pound (/lb) body weight every 12 hours for a maximum of 28 days. Osteomyelitis: 5.0 to 15 mg/lb body weight every 12 hours for a minimum of 28 days.

Antirobe® Capsules

SPL · SPL

FDA Structured Product Label

Antirobe® 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
120-161
Status
RX
Form
Capsule
Route
Oral
Species
Dog
Composition / specifications
Each capsule contains the equivalent of 25, 75, 150 or 300 milligrams of clindamycin as the hydrated hydrochloride salt.

Dogs

Indication

For the treatment of skin infections (wounds and abscesses) due to susceptible strains of coagulase-positive staphylococci (Staphylococcus aureus or S. intermedius), deep wounds and abscesses due to susceptible strains of Bacteroides fragilis, Prevotella melaninogenicus, Fusobacterium necrophorum, and Clostridium perfringens, dental infections due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens, and osteomyelitis due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens.

Dosage

Wounds, abscesses, and dental infections: 2.5 to 15 milligrams per pound of body weight every 12 hours for a maximum of 28 days. Osteomyelitis: 5.0 to 15 milligrams per pound of body weight every 12 hours for a minimum of 28 days.

Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian.

ClindaMed™ Oral Drops

SPL · SPL

FDA Structured Product Label

ClindaMed™ Oral Drops

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
200-538
Status
RX
Form
Liquid
Route
Oral
Species
Dog • Cat
Composition / specifications
Each mL contains clindamycin hydrochloride equivalent to 25 mg clindamycin.

<strong>Dogs</strong>

Indication
For the treatment of infections caused by susceptible strains of the designated microorganisms in the specific conditions listed below:

Skin infections (wounds and abscesses) due to coagulase positive staphylococci (Staphylococcus aureus or Staphylococcus intermedius). Deep wounds and abscesses due to Bacteroides fragilis, Prevotella melaninogenicus, Fusobacterium necrophorum and Clostridium perfringens.

Dental infections due to Staphylococcus aureus, Bacteroides fragilis, Prevotella melaninogenicus, Fusobacterium necrophorum and Clostridium perfringens.

Osteomyelitis due to Staphylococcus aureus, Bacteroides fragilis, Prevotella melaninogenicus, Fusobacterium necrophorum and Clostridium perfringens.

Dosage
Wounds, abscesses, and dental infections: 2.5 to 15 mg per pound body weight every 12 hours for a maximum of 28 days.

Osteomyelitis: 5.0 to 15 mg/lb body weight every 12 hours for a minimum of 28 days.

Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian

<strong>Cats</strong>

Indication
Skin infections (wounds and abscesses) due to Staphylococcus aureus, Staphylococcus intermedius, Streptococcus spp. Deep wounds and abscesses due to Clostridium perfringens and Bacteroides fragilis.

Dental infections due to Staphylococcus aureus, Staphylococcus intermedius, Streptococcus spp., Clostridium perfringens and Bacteroides fragilis.

Dosage
5.0 to 15.0 mg/lb body weight every 24 hours for a maximum of 14 days
Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian

Clindamycin Hydrochloride Oral Drops

SPL · SPL

FDA Structured Product Label

Clindamycin Hydrochloride Oral Drops

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

Sponsor
First Priority, Inc.
ANADA
200-398
Status
RX
Form
Liquid (Solution)
Route
Oral
Species
Dog • Cat
Composition / specifications
Each milliliter of solution contains the equivalent of 25 milligrams (mg) clindamycin as the hydrochloride salt.

Dogs

Indication
For the treatment of skin infections (wounds and abscesses) due to susceptible strains of coagulase-positive staphylococci (Staphylococcus aureus or S. intermedius), deep wounds and abscesses due to susceptible strains of Bacteroides fragilis, Prevotella melaninogenicus, Fusobacterium ecrophorum, and Clostridium perfringens, dental infections due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens, and osteomyelitis due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens
Dosage
Wounds, abscesses, and dental infections: 2.5 to 15 milligrams per pound of body weight every 12 hours for a maximum of 28 days. Osteomyelitis: 5.0 to 15 milligrams per pound of body weight every 12 hours for a minimum of 28 days
Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Cats

Indication
For the treatment of skin infections (wounds and abscesses) due to susceptible strains of S. aureus, S. intermedius, Streptococcus species, deep wounds and abscesses due to susceptible strains of Clostridium perfringens and Bacteroides fragilis, and dental infections due to susceptible strains of S. aureus, S. intermedius, Streptococcus species, C. perfringens, and B. fragilis
Dosage
5.0 to 15.0 milligrams per pound of body weight every 24 hours for a maximum of 14 days.
Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Antirobe Aquadrops®

SPL · SPL

FDA Structured Product Label

Antirobe Aquadrops®

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
135-940
Status
RX
Form
Liquid (Solution)
Route
Oral
Species
Dog • Cat
Composition / specifications
Each milliliter of solution contains the equivalent of 25 milligrams (mg) clindamycin as the hydrochloride salt.

Dogs

Indication

For the treatment of skin infections (wounds and abscesses) due to susceptible strains of coagulase-positive staphylococci (Staphylococcus aureus or S. intermedius), deep wounds and abscesses due to susceptible strains of Bacteroides fragilis, Prevotella melaninogenicus, Fusobacterium necrophorum, and Clostridium perfringens, dental infections due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens, and osteomyelitis due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens.

Dosage
Wounds, abscesses, and dental infections: 2.5 to 15 milligrams per pound of body weight every 12 hours for a maximum of 28 days. Osteomyelitis: 5.0 to 15 milligrams per pound of body weight every 12 hours for a minimum of 28 days.
Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Cats

Indication

For the treatment of skin infections (wounds and abscesses) due to susceptible strains of S. aureus, S. intermedius, Streptococcus species, deep wounds and abscesses due to susceptible strains of Clostridium perfringens and Bacteroides fragilis, and dental infections due to susceptible strains of S. aureus, S. intermedius, Streptococcus species, C. perfringens, and B. fragilis.

Dosage
5.0 to 15.0 milligrams per pound of body weight every 24 hours for a maximum of 14 days.
Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Clindamycin Hydrochloride Oral Liquid

SPL · SPL

FDA Structured Product Label

Clindamycin Hydrochloride Oral Liquid

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
200-193
Status
RX
Form
Liquid (Solution)
Route
Oral
Species
Dog • Cat
Composition / specifications
Each milliliter of 8.64 percent alcoholic solution contains the equivalent of 25 milligrams of clindamycin (as the hydrochloride).

Cats

Indication
Aerobic bacteria: Treatment of soft tissue infections (wounds and abscesses) and dental infections caused by or associated with susceptible strains of Staphylococcus aureus, S. intermedius, and Streptococcus species Anaerobic bacteria: Treatment of soft tissue infections (deep wounds and abscesses) and dental infections caused by or associated with susceptible strains of Clostridium perfringens and Bacteroides fragilis.
Dosage
5.0 to 10.0 milligrams per pound of body weight every 24 hours for a maximum of 14 days (11 to 22 milligrams per kilogram of body weight per day).
Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Dogs

Indication
For treatment of osteomyelitis caused by susceptible strains of Staphylococcus aureus, and osteomyelitis caused by or associated with susceptible strains of Bacteroides fragilis, Bacteroides melaninogenicus, Fusobacterium necrophorum, and Clostridium perfringens.
Dosage
Osteomyelitis: 5.0 milligrams per pound of body weight every 12 hours for a minimum of 28 days.
Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian.
Indication
For use in dogs for treatment of soft tissue infections (wounds and abscesses) and dental infections caused by susceptible strains of Staphylococcus aureus and for soft tissue infections (deep wounds and abscesses) and dental infections caused by or associated with susceptible strains of Bacteroides fragilis, Bacteroides melaninogenicus, Fusobacterium necrophorum, and Clostridium perfringens.
Dosage
Wounds abscesses, and dental infections: 2.5 milligrams per pound of body weight every 12 hours for a maximum of 28 days.
Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Clindamycin Hydrochloride Capsules

SPL · SPL

FDA Structured Product Label

Clindamycin Hydrochloride 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
Cronus Pharma Specialities India Private Ltd.
ANADA
200-298
Status
RX
Form
Capsule
Route
Oral
Species
Dog
Composition / specifications
Each capsule contains the equivalent of 25, 75, or 150 milligrams of clindamycin as the hydrated hydrochloride salt.

Dogs

Indication
For the treatment of skin infections (wounds and abscesses) due to susceptible strains of coagulase-positive staphylococci (Staphylococcus aureus or S. intermedius), deep wounds and abscesses due to susceptible strains of Bacteroides fragilis, Prevotella melaninogenicus, Fusobacterium necrophorum, and Clostridium perfringens, dental infections due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens, and osteomyelitis due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens.
Dosage
Wounds, abscesses, and dental infections: 2.5 milligrams per pound of body weight every 12 hours for a maximum of 28 days. Osteomyelitis: 5.0 milligrams per pound of body weight every 12 hours for a minimum of 28 days.
Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian.

ClindaRobe™

SPL · SPL

FDA Structured Product Label

ClindaRobe™

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

Sponsor
Teva Canada Ltd.
ANADA
200-383
Status
RX
Form
Capsule
Route
Oral
Species
Dog
Composition / specifications
<span style="font-size: 10.5pt; font-family: Verdana; mso-fareast-font-family: 'Times New Roman'; mso-ansi-language: EN-US; mso-fareast-language: EN-US; mso-bidi-language: AR-SA; mso-bidi-font-family: 'Times New Roman'">Each capsule contains the equivalent of 25, 75, or 150 mg of clindamycin.</span>

Dogs

Indication
For the treatment of skin infections (wounds and abscesses) due to susceptible strains of coagulase-positive staphylococci (Staphylococcus aureus or S. intermedius), deep wounds and abscesses due to susceptible strains of Bacteroides fragilis, Prevotella melaninogenicus, Fusobacterium necrophorum, and Clostridium perfringens, dental infections due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens, and osteomyelitis due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens.
Dosage
Wounds, abscesses, and dental infections: 2.5 to 15 milligrams per pound of body weight every 12 hours for a maximum of 28 days. Osteomyelitis: 5.0 to 15 milligrams per pound of body weight every 12 hours for a minimum of 28 days.
Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Clinsol®

SPL · SPL

FDA Structured Product Label

Clinsol®

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

Sponsor
Virbac AH, Inc.
ANADA
200-291
Status
RX
Form
Liquid (Solution)
Route
Oral
Species
Dog • Cat
Composition / specifications
Each milliliter of solution contains the equivalent of 25 milligrams (mg) clindamycin as the hydrochloride salt.

Dogs

Indication
For the treatment of skin infections (wounds and abscesses) due to susceptible strains of coagulase-positive staphylococci (Staphylococcus aureus or (S. intermedius), deep wounds and abscesses due to susceptible strains of (Bacteroides fragilis, (Prevotella melaninogenicus, (Fusobacterium necrophorum, and (Clostridium perfringens; dental infections due to susceptible strains of (S. aureus, (B. fragilis, (P. melaninogenicus, (F. necrophorum, and (C. perfringens; and osteomyelitis due to susceptible strains of (S. aureus, (B. fragilis, (P. melaninogenicus, (F. necrophorum, and (C. perfringens.
Dosage
Wounds, abscesses, and dental infections: 2.5 to 15 milligrams per pound of body weight every 12 hours for a maximum of 28 days. Osteomyelitis: 5.0 to 15 milligrams per pound of body weight every 12 hours for a minimum of 28 days.
Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Cats

Indication
For the treatment of skin infections (wounds and abscesses) due to susceptible strains of Staphylococcus aureus, S. intermedius, Streptococcus spp.; deep wounds and abscesses due to susceptible strains of Clostridium perfringens and Bacteroides fragilis; and dental infections due to susceptible strains of S. aureus, S. intermedius, Streptococcus spp., C. perfringens, and B. fragilis.
Dosage
5.0 to 15.0 milligrams per pound of body weight every 24 hours for a maximum of 14 days.
Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Clintabs®

SPL · SPL

FDA Structured Product Label

Clintabs®

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

Sponsor
Virbac AH, Inc.
ANADA
200-316
Status
RX
Form
Tablet
Route
Oral
Species
Dog
Composition / specifications
Each tablet contains the equivalent of 25, 75 or 150 milligrams of clindamycin as the hydrochloride salt.

Dogs

Indication
For the treatment of skin infections (wounds and abscesses) due to susceptible strains of coagulase-positive staphylococci (Staphylococcus aureus or S. intermedius), deep wounds and abscesses due to susceptible strains of Bacteroides fragilis, Prevotella melaninogenicus, Fusobacterium necrophorum, and Clostridium perfringens, dental infections due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens, and osteomyelitis due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens.
Dosage
Wounds, abscesses, and dental infections: 2.5 to 15 milligrams per pound of body weight every 12 hours for a maximum of 28 days. Osteomyelitis: 5.0 to 15 milligrams per pound of body weight every 12 hours for a minimum of 28 days.
Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Clindamycin Hydrochloride SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Clindamycin Hydrochloride. Use the source link for the full official labeling record.

Clindamycin Hydrochloride SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Clindamycin Hydrochloride. Use the source link for the full official labeling record.

CLINTABS SPL

SPL · Structured Product Label

FDA Structured Product Label XML for CLINTABS. Use the source link for the full official labeling record.

Antirobe SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Antirobe. Use the source link for the full official labeling record.

Antirobe Aquadrops SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Antirobe Aquadrops. Use the source link for the full official labeling record.

ZydaClin SPL

SPL · Structured Product Label

FDA Structured Product Label XML for ZydaClin. Use the source link for the full official labeling record.

Clindamycin SPL

SPL · Structured Product Label

FDA Structured Product Label XML for Clindamycin. Use the source link for the full official labeling record.

FOI Summary oA 200-813 Approved June 27, 2025.pdf

FOI · FOI

ucm069817.pdf

FOI · FOI

UCM355629.pdf

FOI · FOI

ucm061348.pdf

FOI · FOI

ucm069874.pdf

FOI · FOI

UCM454278.pdf

FOI · FOI

N135940_Supp_11_16_89(2).pdf

FOI · FOI

UCM061610.pdf

FOI · FOI

UCM061609.pdf

FOI · FOI

A200193_Org_8_1_1997.pdf

FOI · FOI

ucm061743.pdf

FOI · FOI

ucm061742.pdf

FOI · FOI

ucm061338.pdf

FOI · FOI

ucm061719.pdf

FOI · FOI

ucm061770.pdf

FOI · 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 Aug 6, 2026, 7:47 PM UTC
    The reference fact projection used for browse cards and quick facts.
  • Animal Drugs @ FDA: Source FDA | Refreshed Aug 6, 2026, 7:47 PM 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 Aug 6, 2026, 7:47 PM UTC
    Package/product NDCs from FDA’s electronic listing directory (XLS).
  • openFDA reaction terms: Source FDA openFDA | Refreshed Aug 6, 2026, 7:52 PM UTC
  • openFDA case summaries: Source FDA openFDA | Refreshed Aug 6, 2026, 7:52 PM UTC
Official (FDA)
Identity: Generic ingredient • FDA branded products available
Official FDA brands: Antirobe Antirobe Aquadrops CLINTABS Clindamycin Clindamycin Hydrochloride ZydaClin
Manufacturer mapping: Multiple FDA labelers
Case-reported brands (openFDA): MSK
Catalog species: Both FDA-labeled species: Cat, Dog
Rx/OTC: RX
Form/route: Capsule, Liquid, Liquid (Solution), Tablet Oral
Applications: ANADA 200-813 • NADA 120-161 • ANADA 200-538 • ANADA 200-398 • NADA 135-940 • ANADA 200-193 • ANADA 200-298 • ANADA 200-383 • ANADA 200-291 • ANADA 200-316
NDC: Packages 13985-957-25 51311-400-40 51311-402-75 51311-404-15 54771-3043-1 54771-3044-1 Products 13985 51311 54771 69043 86101 86136
Documents: 15 (FOI: 15) • SPL: 10 Label highlights Official documents
Safety (openFDA)
Top reactions: Dog 110 Cat 51 View
Case summaries: 21 (showing 8) View
openFDA reports are unverified and do not prove causation.

Explore
Linked using: 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
  • Federal law restricts this drug to use by or on the order of a licensed veterinarian. Federal law restricts this drug to use by or on the order of a licensed veterinarian (Contraindication, High)
Top reaction signals
Loss of appetite (1) Diarrhea (1) Dermal thickening (1) Dehydration (1) Decreased cholesterol (1) Decreased appetite (1) Death by euthanasia (1) Death (1)

Identifiers & Packages

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

Identifiers
ANADA: 200193 ANADA: 200291 ANADA: 200298 ANADA: 200316 ANADA: 200383 ANADA: 200398 ANADA: 200538 ANADA: 200813 NADA: 120161 NADA: 135940 NDC Package: 13985-957-25 NDC Package: 51311-400-40 NDC Package: 51311-402-75 NDC Package: 51311-404-15 NDC Package: 54771-3043-1 NDC Package: 54771-3044-1 NDC Package: 54771-3045-1 NDC Package: 54771-3179-1 NDC Package: 54771-3179-2 NDC Package: 69043-013-20 NDC Package: 69043-014-20 NDC Package: 69043-015-01 NDC Package: 69043-015-05 NDC Package: 69043-016-01
Package NDC Product NDC Form / Route Status
13985-957-25 13985 -
51311-400-40 51311 -
51311-402-75 51311 -
51311-404-15 51311 -
54771-3043-1 54771 -
54771-3044-1 54771 -
54771-3045-1 54771 -
54771-3179-1 54771 -
54771-3179-2 54771 -
69043-013-20 69043 -
69043-014-20 69043 -
69043-015-01 69043 -
69043-015-05 69043 -
69043-016-01 69043 -
86101-052-18 86101 -
86101-053-15 86101 -
86101-054-11 86101 -
86136-147-03 86136 -
86136-148-03 86136 -

Enriched Documents

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

  • Clindamycin Hydrochloride SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • Clindamycin Hydrochloride SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • CLINTABS SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • Antirobe SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • Antirobe Aquadrops SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • ZydaClin SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • Clindamycin SPL • Structured Product Label • Official
    FDA Structured Product Label from the electronic animal drug product listing directory.
  • FOI Summary oA 200-813 Approved June 27, 2025.pdf • FOI summary • Official • July 1, 2025
    FDA FOI summary for application 200813
  • ucm069817.pdf • FOI summary • Official • Dec. 10, 2019
    FDA FOI summary for application 120161
  • UCM355629.pdf • FOI summary • Official • Oct. 2, 2018
    FDA FOI summary for application 200538
  • ucm061348.pdf • FOI summary • Official • Dec. 27, 2017
    FDA FOI summary for application 200398
  • N135940_Supp_11_16_89(2).pdf • FOI summary • Official • July 11, 2017
    FDA FOI summary for application 135940
  • UCM454278.pdf • FOI summary • Official • July 11, 2017
    FDA FOI summary for application 135940
  • ucm069874.pdf • FOI summary • Official • July 11, 2017
    FDA FOI summary for application 135940
  • A200193_Org_8_1_1997.pdf • FOI summary • Official • May 22, 2017
    FDA FOI summary for application 200193
  • UCM061609.pdf • FOI summary • Official • May 22, 2017
    FDA FOI summary for application 200193
  • UCM061610.pdf • FOI summary • Official • May 22, 2017
    FDA FOI summary for application 200193
  • ucm061338.pdf • FOI summary • Official • June 1, 2016
    FDA FOI summary for application 200383
  • ucm061770.pdf • FOI summary • Official • June 1, 2016
    FDA FOI summary for application 200316
  • ucm061742.pdf • FOI summary • Official • June 1, 2016
    FDA FOI summary for application 200298
  • ucm061743.pdf • FOI summary • Official • June 1, 2016
    FDA FOI summary for application 200298
  • ucm061719.pdf • FOI summary • Official • June 1, 2016
    FDA FOI summary for application 200291

Data Sources & Change Log

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

Official 141 Clinical 1 Manufacturer 0 Marketing 0
Current Field Facts
  • side_effects: Top reported reactions (openFDA): Vomiting, Death by euthanasia, Lethargy (see also Central nervous system depression in 'Neurological'), Anorexia, Other abnor… (Clinical, 2026-04-11)
  • contraindications: Federal law restricts this drug to use by or on the order of a licensed veterinarian. Federal law restricts this drug to use by or on the order of a licensed v… (Official, 2026-04-12)
  • contraindications: Federal law restricts this drug to use by or on the order of a licensed veterinarian. Federal law restricts this drug to use by or on the order of a licensed v… (Official, 2026-04-11)
  • contraindications: Federal law restricts this drug to use by or on the order of a licensed veterinarian. Federal law restricts this drug to use by or on the order of a licensed v… (Official, 2026-02-12)
  • indications: CLINDAROBE Capsules is indicated for the treatment of infections caused by susceptible strains of the designated microorganisms in the specific conditions list… (Official, 2026-08-06)
  • indications: CLINDAROBE Capsules is indicated for the treatment of infections caused by susceptible strains of the designated microorganisms in the specific conditions list… (Official, 2026-08-05)
  • indications: CLINDAROBE Capsules is indicated for the treatment of infections caused by susceptible strains of the designated microorganisms in the specific conditions list… (Official, 2026-08-04)
  • indications: CLINDAROBE Capsules is indicated for the treatment of infections caused by susceptible strains of the designated microorganisms in the specific conditions list… (Official, 2026-08-03)
  • indications: CLINDAROBE Capsules is indicated for the treatment of infections caused by susceptible strains of the designated microorganisms in the specific conditions list… (Official, 2026-08-02)
  • indications: CLINDAROBE Capsules is indicated for the treatment of infections caused by susceptible strains of the designated microorganisms in the specific conditions list… (Official, 2026-08-01)
  • indications: CLINDAROBE Capsules is indicated for the treatment of infections caused by susceptible strains of the designated microorganisms in the specific conditions list… (Official, 2026-07-31)
  • indications: CLINDAROBE Capsules is indicated for the treatment of infections caused by susceptible strains of the designated microorganisms in the specific conditions list… (Official, 2026-07-30)
  • indications: CLINDAROBE Capsules is indicated for the treatment of infections caused by susceptible strains of the designated microorganisms in the specific conditions list… (Official, 2026-07-29)
  • indications: CLINDAROBE Capsules is indicated for the treatment of infections caused by susceptible strains of the designated microorganisms in the specific conditions list… (Official, 2026-07-28)
  • indications: CLINDAROBE Capsules is indicated for the treatment of infections caused by susceptible strains of the designated microorganisms in the specific conditions list… (Official, 2026-07-27)
  • indications: CLINDAROBE Capsules is indicated for the treatment of infections caused by susceptible strains of the designated microorganisms in the specific conditions list… (Official, 2026-07-26)
  • indications: CLINDAROBE Capsules is indicated for the treatment of infections caused by susceptible strains of the designated microorganisms in the specific conditions list… (Official, 2026-07-25)
  • indications: CLINDAROBE Capsules is indicated for the treatment of infections caused by susceptible strains of the designated microorganisms in the specific conditions list… (Official, 2026-07-25)
  • indications: CLINDAROBE Capsules is indicated for the treatment of infections caused by susceptible strains of the designated microorganisms in the specific conditions list… (Official, 2026-07-22)
  • indications: CLINDAROBE Capsules is indicated for the treatment of infections caused by susceptible strains of the designated microorganisms in the specific conditions list… (Official, 2026-07-22)
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
Clindamycin Hydrochloride Tablets
RX
Clindamycin Hydrochloride
Tablet Oral
Felix Pharmaceuticals Pvt. Ltd. ANADA 200-813 Approved Jul 1, 2025
Antirobe® Capsules
RX
Clindamycin Hydrochloride
Capsule Oral
Zoetis Inc. NADA 120-161 Approved Dec 10, 2019
ClindaMed™ Oral Drops
RX
Clindamycin
Liquid Oral
Bimeda Animal Health Ltd. ANADA 200-538 Approved Oct 2, 2018
Clindamycin Hydrochloride Oral Drops
RX
Clindamycin Hydrochloride
Liquid (Solution) Oral
First Priority, Inc. ANADA 200-398 Approved Dec 27, 2017
Antirobe Aquadrops®
RX
Clindamycin Hydrochloride
Liquid (Solution) Oral
Zoetis Inc. NADA 135-940 Approved Jul 11, 2017
Clindamycin Hydrochloride Oral Liquid
RX
Clindamycin Hydrochloride
Liquid (Solution) Oral
Cronus Pharma Specialities India Private Ltd. ANADA 200-193 Approved May 22, 2017
Clindamycin Hydrochloride Capsules
RX
Clindamycin Hydrochloride
Capsule Oral
Cronus Pharma Specialities India Private Ltd. ANADA 200-298 Approved Jun 1, 2016
ClindaRobe™
RX
Clindamycin Hydrochloride
Capsule Oral
Teva Canada Ltd. ANADA 200-383 W Jun 1, 2016
Clinsol®
RX
Clindamycin Hydrochloride
Liquid (Solution) Oral
Virbac AH, Inc. ANADA 200-291 Approved Jun 1, 2016
Clintabs®
RX
Clindamycin Hydrochloride
Tablet Oral
Virbac AH, Inc. ANADA 200-316 Approved 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.

Composition / specifications
25 mg, 75 mg, and 150 mg
Dogs
Indication

For the treatment of skin infections (wounds and abscesses) due to susceptible strains of coagulase-positive staphylococci (Staphylococcus aureus or S. intermedius), deep wounds and abscesses due to susceptible strains of Bacteroides fragilis, Prevotella melaninogenicus, Fusobacterium necrophorum, and Clostridium perfringens, dental infections due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens, and osteomyelitis due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens.

Dosage

Wounds, abscesses, and dental infections: 2.5 to 15 mg per pound (/lb) body weight every 12 hours for a maximum of 28 days. Osteomyelitis: 5.0 to 15 mg/lb body weight every 12 hours for a minimum of 28 days.

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: Dog
Composition / specifications
Each capsule contains the equivalent of 25, 75, 150 or 300 milligrams of clindamycin as the hydrated hydrochloride salt.
Dogs
Indication

For the treatment of skin infections (wounds and abscesses) due to susceptible strains of coagulase-positive staphylococci (Staphylococcus aureus or S. intermedius), deep wounds and abscesses due to susceptible strains of Bacteroides fragilis, Prevotella melaninogenicus, Fusobacterium necrophorum, and Clostridium perfringens, dental infections due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens, and osteomyelitis due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens.

Dosage

Wounds, abscesses, and dental infections: 2.5 to 15 milligrams per pound of body weight every 12 hours for a maximum of 28 days. Osteomyelitis: 5.0 to 15 milligrams per pound of body weight every 12 hours for a minimum of 28 days.

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: Dog • Cat
Composition / specifications
Each mL contains clindamycin hydrochloride equivalent to 25 mg clindamycin.
<strong>Dogs</strong>
Indication
For the treatment of infections caused by susceptible strains of the designated microorganisms in the specific conditions listed below:

Skin infections (wounds and abscesses) due to coagulase positive staphylococci (Staphylococcus aureus or Staphylococcus intermedius). Deep wounds and abscesses due to Bacteroides fragilis, Prevotella melaninogenicus, Fusobacterium necrophorum and Clostridium perfringens.

Dental infections due to Staphylococcus aureus, Bacteroides fragilis, Prevotella melaninogenicus, Fusobacterium necrophorum and Clostridium perfringens.

Osteomyelitis due to Staphylococcus aureus, Bacteroides fragilis, Prevotella melaninogenicus, Fusobacterium necrophorum and Clostridium perfringens.

Dosage
Wounds, abscesses, and dental infections: 2.5 to 15 mg per pound body weight every 12 hours for a maximum of 28 days.

Osteomyelitis: 5.0 to 15 mg/lb body weight every 12 hours for a minimum of 28 days.

Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian
<strong>Cats</strong>
Indication
Skin infections (wounds and abscesses) due to Staphylococcus aureus, Staphylococcus intermedius, Streptococcus spp. Deep wounds and abscesses due to Clostridium perfringens and Bacteroides fragilis.

Dental infections due to Staphylococcus aureus, Staphylococcus intermedius, Streptococcus spp., Clostridium perfringens and Bacteroides fragilis.

Dosage
5.0 to 15.0 mg/lb body weight every 24 hours for a maximum of 14 days
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: Dog • Cat
Composition / specifications
Each milliliter of solution contains the equivalent of 25 milligrams (mg) clindamycin as the hydrochloride salt.
Dogs
Indication
For the treatment of skin infections (wounds and abscesses) due to susceptible strains of coagulase-positive staphylococci (Staphylococcus aureus or S. intermedius), deep wounds and abscesses due to susceptible strains of Bacteroides fragilis, Prevotella melaninogenicus, Fusobacterium ecrophorum, and Clostridium perfringens, dental infections due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens, and osteomyelitis due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens
Dosage
Wounds, abscesses, and dental infections: 2.5 to 15 milligrams per pound of body weight every 12 hours for a maximum of 28 days. Osteomyelitis: 5.0 to 15 milligrams per pound of body weight every 12 hours for a minimum of 28 days
Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian.
Cats
Indication
For the treatment of skin infections (wounds and abscesses) due to susceptible strains of S. aureus, S. intermedius, Streptococcus species, deep wounds and abscesses due to susceptible strains of Clostridium perfringens and Bacteroides fragilis, and dental infections due to susceptible strains of S. aureus, S. intermedius, Streptococcus species, C. perfringens, and B. fragilis
Dosage
5.0 to 15.0 milligrams per pound of body weight every 24 hours for a maximum of 14 days.
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: Dog • Cat
Composition / specifications
Each milliliter of solution contains the equivalent of 25 milligrams (mg) clindamycin as the hydrochloride salt.
Dogs
Indication

For the treatment of skin infections (wounds and abscesses) due to susceptible strains of coagulase-positive staphylococci (Staphylococcus aureus or S. intermedius), deep wounds and abscesses due to susceptible strains of Bacteroides fragilis, Prevotella melaninogenicus, Fusobacterium necrophorum, and Clostridium perfringens, dental infections due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens, and osteomyelitis due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens.

Dosage
Wounds, abscesses, and dental infections: 2.5 to 15 milligrams per pound of body weight every 12 hours for a maximum of 28 days. Osteomyelitis: 5.0 to 15 milligrams per pound of body weight every 12 hours for a minimum of 28 days.
Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian.
Cats
Indication

For the treatment of skin infections (wounds and abscesses) due to susceptible strains of S. aureus, S. intermedius, Streptococcus species, deep wounds and abscesses due to susceptible strains of Clostridium perfringens and Bacteroides fragilis, and dental infections due to susceptible strains of S. aureus, S. intermedius, Streptococcus species, C. perfringens, and B. fragilis.

Dosage
5.0 to 15.0 milligrams per pound of body weight every 24 hours for a maximum of 14 days.
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: Dog • Cat
Composition / specifications
Each milliliter of 8.64 percent alcoholic solution contains the equivalent of 25 milligrams of clindamycin (as the hydrochloride).
Cats
Indication
Aerobic bacteria: Treatment of soft tissue infections (wounds and abscesses) and dental infections caused by or associated with susceptible strains of Staphylococcus aureus, S. intermedius, and Streptococcus species Anaerobic bacteria: Treatment of soft tissue infections (deep wounds and abscesses) and dental infections caused by or associated with susceptible strains of Clostridium perfringens and Bacteroides fragilis.
Dosage
5.0 to 10.0 milligrams per pound of body weight every 24 hours for a maximum of 14 days (11 to 22 milligrams per kilogram of body weight per day).
Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian.
Dogs
Indication
For treatment of osteomyelitis caused by susceptible strains of Staphylococcus aureus, and osteomyelitis caused by or associated with susceptible strains of Bacteroides fragilis, Bacteroides melaninogenicus, Fusobacterium necrophorum, and Clostridium perfringens.
Dosage
Osteomyelitis: 5.0 milligrams per pound of body weight every 12 hours for a minimum of 28 days.
Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian.
Indication
For use in dogs for treatment of soft tissue infections (wounds and abscesses) and dental infections caused by susceptible strains of Staphylococcus aureus and for soft tissue infections (deep wounds and abscesses) and dental infections caused by or associated with susceptible strains of Bacteroides fragilis, Bacteroides melaninogenicus, Fusobacterium necrophorum, and Clostridium perfringens.
Dosage
Wounds abscesses, and dental infections: 2.5 milligrams per pound of body weight every 12 hours for a maximum of 28 days.
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: Dog
Composition / specifications
Each capsule contains the equivalent of 25, 75, or 150 milligrams of clindamycin as the hydrated hydrochloride salt.
Dogs
Indication
For the treatment of skin infections (wounds and abscesses) due to susceptible strains of coagulase-positive staphylococci (Staphylococcus aureus or S. intermedius), deep wounds and abscesses due to susceptible strains of Bacteroides fragilis, Prevotella melaninogenicus, Fusobacterium necrophorum, and Clostridium perfringens, dental infections due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens, and osteomyelitis due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens.
Dosage
Wounds, abscesses, and dental infections: 2.5 milligrams per pound of body weight every 12 hours for a maximum of 28 days. Osteomyelitis: 5.0 milligrams per pound of body weight every 12 hours for a minimum of 28 days.
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: Dog
Composition / specifications
<span style="font-size: 10.5pt; font-family: Verdana; mso-fareast-font-family: 'Times New Roman'; mso-ansi-language: EN-US; mso-fareast-language: EN-US; mso-bidi-language: AR-SA; mso-bidi-font-family: 'Times New Roman'">Each capsule contains the equivalent of 25, 75, or 150 mg of clindamycin.</span>
Dogs
Indication
For the treatment of skin infections (wounds and abscesses) due to susceptible strains of coagulase-positive staphylococci (Staphylococcus aureus or S. intermedius), deep wounds and abscesses due to susceptible strains of Bacteroides fragilis, Prevotella melaninogenicus, Fusobacterium necrophorum, and Clostridium perfringens, dental infections due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens, and osteomyelitis due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens.
Dosage
Wounds, abscesses, and dental infections: 2.5 to 15 milligrams per pound of body weight every 12 hours for a maximum of 28 days. Osteomyelitis: 5.0 to 15 milligrams per pound of body weight every 12 hours for a minimum of 28 days.
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: Dog • Cat
Composition / specifications
Each milliliter of solution contains the equivalent of 25 milligrams (mg) clindamycin as the hydrochloride salt.
Dogs
Indication
For the treatment of skin infections (wounds and abscesses) due to susceptible strains of coagulase-positive staphylococci (Staphylococcus aureus or (S. intermedius), deep wounds and abscesses due to susceptible strains of (Bacteroides fragilis, (Prevotella melaninogenicus, (Fusobacterium necrophorum, and (Clostridium perfringens; dental infections due to susceptible strains of (S. aureus, (B. fragilis, (P. melaninogenicus, (F. necrophorum, and (C. perfringens; and osteomyelitis due to susceptible strains of (S. aureus, (B. fragilis, (P. melaninogenicus, (F. necrophorum, and (C. perfringens.
Dosage
Wounds, abscesses, and dental infections: 2.5 to 15 milligrams per pound of body weight every 12 hours for a maximum of 28 days. Osteomyelitis: 5.0 to 15 milligrams per pound of body weight every 12 hours for a minimum of 28 days.
Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian.
Cats
Indication
For the treatment of skin infections (wounds and abscesses) due to susceptible strains of Staphylococcus aureus, S. intermedius, Streptococcus spp.; deep wounds and abscesses due to susceptible strains of Clostridium perfringens and Bacteroides fragilis; and dental infections due to susceptible strains of S. aureus, S. intermedius, Streptococcus spp., C. perfringens, and B. fragilis.
Dosage
5.0 to 15.0 milligrams per pound of body weight every 24 hours for a maximum of 14 days.
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: Dog
Composition / specifications
Each tablet contains the equivalent of 25, 75 or 150 milligrams of clindamycin as the hydrochloride salt.
Dogs
Indication
For the treatment of skin infections (wounds and abscesses) due to susceptible strains of coagulase-positive staphylococci (Staphylococcus aureus or S. intermedius), deep wounds and abscesses due to susceptible strains of Bacteroides fragilis, Prevotella melaninogenicus, Fusobacterium necrophorum, and Clostridium perfringens, dental infections due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens, and osteomyelitis due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens.
Dosage
Wounds, abscesses, and dental infections: 2.5 to 15 milligrams per pound of body weight every 12 hours for a maximum of 28 days. Osteomyelitis: 5.0 to 15 milligrams per pound of body weight every 12 hours for a minimum of 28 days.
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

For the treatment of skin infections (wounds and abscesses) due to susceptible strains of coagulase-positive staphylococci ( Staphylococcus aureus or S. intermedius ), deep wounds and abscesses due to susceptible strains of Bacteroides fragilis , Prevotella melaninogenicus , Fusobacterium necrophorum , and Clostridium perfringens , dental infections due to susceptible strains of S. aureus , B. fragilis , P. melaninogenicus , F. necrophorum , and C. perfringens , and osteomyelitis due to susceptible strains of S. aureus , B. fragilis , P. melaninogenicus , F. necrophorum , and C. perfringens . For the treatment of skin infections (wounds and abscesses) due to susceptible strains of coagulase-positive staphylococci ( Staphylococcus aureus or S. intermedius ), deep wounds and abscesses due to susceptible strains of Bacteroides fragilis , Prevotella melaninogenicus, Fusobacterium necrophorum , and Clostridium perfringens , dental infections due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens , and osteomyelitis due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum , and C. perfringens . For the treatment of skin infections (wounds and abscesses) due to susceptible strains of S. aureus, S. intermedius, Streptococcus species, deep wounds and abscesses due to susceptible strains of Clostridium perfringens and Bacteroides fragilis , and dental infections due to susceptible strains of S. aureus, S. intermedius, Streptococcus species, C. perfringens , and B. fragilis .

Source: FDA Animal Drugs @ FDA • Reference

Contraindications

Federal law restricts this drug to use by or on the order of a licensed veterinarian. Federal law restricts this drug to use by or on the order of a licensed veterinarian

Top Reported Reactions (openFDA)

De-duplicated reaction terms grouped by body system from FDA openFDA reports (not verified; does not prove causation).

Digestive
Loss of appetite (1) • Dog Diarrhea (1) • Dog Decreased appetite (1) • Dog

Showing top 5 for Digestive.

Skin & allergy
Application site hair loss (1) • Cat

Showing top 5 for Skin & allergy.

Neurologic
Unsteady walking (1) • Dog Circling - neurological disorder (1) • Dog

Showing top 5 for Neurologic.

Behavior
Behavioral disorder (1) • Cat

Showing top 5 for Behavior.

Other
Difficulty standing (1) • Dog Difficulty going up/down stairs (1) • Dog Dermal thickening (1) • Dog Dehydration (1) • Dog Decreased cholesterol (1) • Dog
Show more (20)
Death by euthanasia (1) • Cat Death (1) • Dog Cyanotic mucous membranes (1) • Dog Corneal ulcer (1) • Dog Corneal oedema (1) • Dog Corneal disorder NOS (1) • Dog Conjunctival oedema (1) • Dog Confusion (1) • Dog Collapse of leg (1) • Dog Collapse NOS (1) • Dog Cold feeling of extremity (1) • Dog Coagulopathy (1) • Dog Cardiac arrest (1) • Cat Azotaemia (1) • Dog Aspiration pneumonia (1) • Dog Application site excoriation (1) • Cat Abnormal red blood cell (1) • Dog Abnormal menace reflex test (1) • Dog Abnormal cytology (1) • Dog Abdominal effusion (1) • 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, Schnauzer - Miniature, Male, 14 year, 7.212 kilogram • Drug: MSK, Unassigned, Unknown • Reactions: Unsteady walking (ataxia), Collapse of leg, Elevated blood urea nitrogen, Elevated cholesterol, Weakness… • Outcome: Ongoing

  • Report ID: USA-USFDACVM-2026-US-014603
  • Serious AE: No
  • Treated For AE: No
  • Sex: Male
  • Age: 14.00 Year
  • Weight: 7.212 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Unknown
  • Form: Unassigned
Reactions Reported:
Unsteady walking (ataxia) Collapse of leg Elevated blood urea nitrogen Elevated cholesterol Weakness Confusion Hyperphosphataemia Elevated symmetrical dimethylarginine Hind limb ataxia Difficulty standing Difficulty going up/down stairs Circling - neurological disorder
Outcomes: Ongoing

Cat, Domestic Shorthair, Female, 2 year, 4.53 kilogram • Drug: MSK, Unknown • Reactions: Limb amputation, Injection site sarcoma, Behavioral disorder (unspecified), Tiredness (lethargy), Localised pain NOS… • Outcome: Outcome Unknown

  • Report ID: USA-USFDACVM-2026-US-014257
  • Serious AE: Yes
  • Treated For AE: Yes
  • Sex: Female
  • Age: 2.00 Year
  • Weight: 4.530 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Unknown
Reactions Reported:
Limb amputation Injection site sarcoma Behavioral disorder (unspecified) Tiredness (lethargy) Localised pain NOS Vocalisation Limping Injection site mass NOS
Outcomes: Outcome Unknown

Cat, Domestic Shorthair, Female, 7 year, 4.354 kilogram • Drug: MSK, Solution/drops, Oral • Reactions: Drooling, Reluctant to move, Not eating, Dilated pupils, Not himself/herself… • Outcome: Died

  • Report ID: USA-USFDACVM-2026-US-014092
  • Serious AE: Yes
  • Treated For AE: Yes
  • Sex: Female
  • Age: 7.00 Year
  • Weight: 4.354 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Oral
  • Form: Solution/drops
Reactions Reported:
Drooling Reluctant to move Not eating Dilated pupils Not himself/herself Hypothermia Tachypnoea Intentional misuse Leukopenia NOS Hypoglycaemia Elevated symmetrical dimethylarginine Azotaemia Low ionized calcium Obtunded Weak pulse Lateral recumbency Regurgitation Cardiac arrest Death
Outcomes: Died

Cat, Domestic Shorthair, Female, 13 year, 6.427 kilogram • Drug: MSK, Unknown • Reactions: Itching, Skin lesion NOS, Skin scab • Outcome: Ongoing

  • Report ID: USA-USFDACVM-2026-US-013313
  • Serious AE: Yes
  • Treated For AE: Yes
  • Sex: Female
  • Age: 13.00 Year
  • Weight: 6.427 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Unknown
Reactions Reported:
Itching Skin lesion NOS Skin scab
Outcomes: Ongoing

Dog, Samoyed, Male, 9 year, 24.948 kilogram • Drug: MSK, Oral • Reactions: Tiredness (lethargy), Shaking, Pale mucous membrane, Cold feeling of extremity, Vomiting… • Outcome: Ongoing

  • Report ID: USA-USFDACVM-2026-US-013066
  • Serious AE: Yes
  • Treated For AE: Yes
  • Sex: Male
  • Age: 9.00 Year
  • Weight: 24.948 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Oral
Reactions Reported:
Tiredness (lethargy) Shaking Pale mucous membrane Cold feeling of extremity Vomiting Tachycardia Laboured breathing Tachypnoea Dehydration Weak pulse Tense abdomen Hypochloraemia Hyponatremia Azotaemia Hypocalcaemia Hypoglycaemia Hyperphosphataemia Hypoproteinaemia Hypoalbuminaemia Low alanine aminotransferase Elevated lactate Increased percentage reticulocytes Lymphocytosis Monocytosis Abnormal red blood cell Hypotension Abdominal effusion Aspiration pneumonia Heart murmur Gastric perforation Lateral recumbency Septicaemia Coagulopathy Hypernatraemia Hypercalcaemia Elevated serum alkaline phosphatase Neutrophilia Stridor Unresponsive to stimuli Cyanotic mucous membranes Thrombosis Oedema of the extremities Pitting oedema Lameness Elevated aspartate aminotransferase Stertor
Outcomes: Ongoing

Dog, Schnauzer - Miniature, Male, 14 year, 7.212 kilogram • Drug: MSK, Solution/drops, Unknown • Reactions: Unsteady walking (ataxia), Collapse of leg, Elevated blood urea nitrogen, Elevated cholesterol, Weakness… • Outcome: Ongoing

  • Report ID: USA-USFDACVM-2026-US-012493
  • Serious AE: No
  • Treated For AE: No
  • Sex: Male
  • Age: 14.00 Year
  • Weight: 7.212 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Unknown
  • Form: Solution/drops
Reactions Reported:
Unsteady walking (ataxia) Collapse of leg Elevated blood urea nitrogen Elevated cholesterol Weakness Confusion Hyperphosphataemia Elevated symmetrical dimethylarginine
Outcomes: Ongoing

Cat, Domestic Shorthair, Female, 13 year, 6.427 kilogram • Drug: MSK, Unassigned, Unknown • Reactions: Itching, Skin lesion NOS, Skin scab, Labeled drug-species interaction, Intentional misuse • Outcome: Ongoing

  • Report ID: USA-USFDACVM-2026-US-010698
  • Serious AE: No
  • Treated For AE: Yes
  • Sex: Female
  • Age: 13.00 Year
  • Weight: 6.427 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Unknown
  • Form: Unassigned
Reactions Reported:
Itching Skin lesion NOS Skin scab Labeled drug-species interaction Intentional misuse
Outcomes: Ongoing

Cat, Domestic Shorthair, Female, 8 year, 4.98 kilogram • Drug: MSK, Unknown • Reactions: Dilated pupils, Hyperactivity, Quiet • Outcome: Ongoing

  • Report ID: USA-USFDACVM-2026-US-007430
  • Serious AE: No
  • Treated For AE: Yes
  • Sex: Female
  • Age: 8.00 Year
  • Weight: 4.980 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Unknown
Reactions Reported:
Dilated pupils Hyperactivity Quiet
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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