Skip to main content
Start triage

Start triage first, then route to emergency care.

Need urgent help? Start triage first, then route to emergency care.

Meds A-Z

Cefovecin Sodium

Detailed information about Cefovecin Sodium

Official label facts Owner quick guide first Marketing clearly labeled

Veterinary professional?

Showing simplified owner view. Switch to Vet View for full technical detail.

Add to My Pet's Meds

Choose a pet, confirm current or past, and optionally add reminder notes.

Sign in to save this medication to your pet profile.

Sign in to continue

Reviewed / Updated / Sources

Reviewed: Not available

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

Sources:

Pet Owner Quick Guide

Start here first for the simple next-step summary.

Used for:

For the treatment of skin infections (secondary superficial pyoderma, abscesses, and wounds) in dogs caused by susceptible strains of Staphylococcus intermedius and Streptococcus canis (Group G).

What to watch for:

  • For subcutaneous use in dogs and cats only
  • Maximum treatment should not exceed 2 injections
  • Low blood pressure (1 reports)
  • Local erythema (1 reports)
  • Lack of efficacy - NOS (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 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?
Safety & side effects

What to watch:

  • For subcutaneous use in dogs and cats only
  • Maximum treatment should not exceed 2 injections
  • Low blood pressure
  • Local erythema
  • Lack of efficacy - NOS

Most reported reactions:

  • Low blood pressure (1 reports)
  • Local erythema (1 reports)
  • Lack of efficacy - NOS (1 reports)

When to call your vet:

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

Data freshness: source data appears current.

Latest refresh: Mar 21, 2026, 10:02 a.m.

Data freshness
  • Medication catalog: Source Roxee | Refreshed Feb 12, 2026, 10:44 PM UTC
  • Animal Drugs @ FDA: Source FDA | Refreshed Mar 21, 2026, 10:00 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 Mar 21, 2026, 10:01 AM UTC
    Package/product NDCs from FDA’s electronic listing directory (XLS).
  • openFDA reaction terms: Source FDA openFDA | Refreshed Mar 21, 2026, 10:02 AM UTC
  • openFDA case summaries: Source FDA openFDA | Refreshed Feb 9, 2026, 3:20 AM UTC
Image coming soon
Cefovecin Sodium

Cefovecin Sodium

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

Species: Both

Manufacturer: Not available (source)

Quick Facts

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

Species: Both
Manufacturer: Not available
Form: Lyophilized powder for injection, Powder
Identifiers:
ANADA: 200812 NADA: 141285 NDC Package: 17033-002-01 NDC Package: 54771-1520-1 NDC Product: 17033 NDC Product: 54771
Source metadata:

Warnings / Contraindications

Federal law restricts this drug to use by or on the order of a licensed veterinarian. For subcutaneous use in dogs and cats only. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Maximum treatment should not exceed 2 injections. For subcutaneous use in dogs and cats only.

  • High: Federal law restricts this drug to use by or on the order of a licensed veterinarian. For subcutaneous use in dogs and cats only. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Maximum treatment should not exceed 2 injections. For subcutaneous use in dogs and cats only.
Source metadata:

Adverse Reactions

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

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

Tracked signals
32
Reported cases
32
Serious reports
18
Species represented
2
Grouped by Body System
Digestive (3) · Loss of appetite, Diarrhea, Decreased appetite Skin & allergy (2) · Hives, Facial swelling (possible allergy) Neurologic (2) · Unsteady walking (ataxia), Tiredness (lethargy) Effectiveness (1) · Lack of efficacy - NOS Other (24) · Low blood pressure, Local erythema, Ketosis
Most Reported Reactions
Reaction Body system Cases Species Serious cases
Other 1 Dog 1
Other 1 Dog 1
Effectiveness 1 Dog 1
Other 1 Dog 1
Other 1 Dog 1
Other 1 Dog 1
Skin & allergy 1 Dog 1
Other 1 Dog 1

Species coverage: Dog (21) Cat (11)

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

Documents

Owner handouts and official technical documents are grouped for faster access.

Owner handouts (0)
  • No owner handouts linked yet.
Official label / PI (0)
  • No official label or package insert links yet.
SPL (2)
  • Cefovecin Sodium for Injection · SPL
    https://animaldrugsatfda.fda.gov/adafda/app/search/public/spl/file/17466/Cefovecin%20Sodium%20for%20Injection
  • Convenia® · SPL
    https://animaldrugsatfda.fda.gov/adafda/app/search/public/spl/file/171/Convenia%C2%AE
FOI (2)
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
  • Medication catalog: Source Roxee | Refreshed Feb 12, 2026, 10:44 PM UTC
  • Animal Drugs @ FDA: Source FDA | Refreshed Mar 21, 2026, 10:00 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 Mar 21, 2026, 10:01 AM UTC
    Package/product NDCs from FDA’s electronic listing directory (XLS).
  • openFDA reaction terms: Source FDA openFDA | Refreshed Mar 21, 2026, 10:02 AM UTC
  • openFDA case summaries: Source FDA openFDA | Refreshed Feb 9, 2026, 3:20 AM UTC
Official (FDA)
Identity: Generic ingredient • FDA branded products available
Official FDA brands: Cefovecin Sodium for Injection Convenia®
Case-reported brands (openFDA): MSK
Catalog species: Both FDA-labeled species: Cat, Dog
Rx/OTC: RX
Form/route: Lyophilized powder for injection, Powder Subcutaneous
Applications: ANADA 200-812 • NADA 141-285
Documents: 2 (FOI: 2) • SPL: 2 Label highlights Official documents
Safety (openFDA)
Top reactions: Dog 14 Cat 19 View
Case summaries: 10 (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. For subcutaneous use in dogs and cats only. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Maximum treatment should not exceed 2 injections. For subcutaneous use in dogs and cats only. (Contraindication, High)
Top reaction signals
Low blood pressure (1) Local erythema (1) Lack of efficacy - NOS (1) Jaundice (1) Hypokalaemia (1) Hyperpigmentation (1) Hives (1) Glomerulonephritis (1)

Identifiers & Packages

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

Identifiers
ANADA: 200812 NADA: 141285 NDC Package: 17033-002-01 NDC Package: 54771-1520-1 NDC Product: 17033 NDC Product: 54771
Package NDC Product NDC Form / Route Status
17033-002-01 17033 -
54771-1520-1 54771 -

Enriched Documents

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

Data Sources & Change Log

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

Official 5 Clinical 0 Manufacturer 0 Marketing 0
Current Field Facts
  • contraindications: Federal law restricts this drug to use by or on the order of a licensed veterinarian. For subcutaneous use in dogs and cats only. Federal law restricts this dr… (Official, 2026-02-12)
  • side_effects: Top reported reactions (openFDA): Vomiting, Corneal ulcer, Other abnormal test result NOS, Diarrhoea, Lethargy (see also Central nervous system depression in '… (Official, 2026-02-12)
  • usage: For the treatment of skin infections (wounds and abscesses) in cats caused by susceptible strains of Pasteurella multocida . For the treatment of skin infectio… (Official, 2026-02-12)
Recent Revisions
  • 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
Cefovecin Sodium for Injection
RX
Cefovecin sodium
Lyophilized powder for injection Subcutaneous
Qilu Animal Health Products Co., Ltd. ANADA 200-812 Approved Jul 1, 2025
Convenia®
RX
Cefovecin sodium
Powder Subcutaneous
Zoetis Inc. NADA 141-285 Approved Oct 2, 2017

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 mL of reconstituted lyophile contains 80 mg of cefovecin as the sodium salt
Dogs
Indication

For the treatment of skin infections (secondary superficial pyoderma, abscesses, and wounds) in dogs caused by susceptible strains of Staphylococcus intermedius and Streptococcus canis (Group G).

Dosage

Administer 3.6 mg/pound (lb) (8 mg/kilograms (kg)) body weight as a single subcutaneous injection. A second subcutaneous injection of 3.6 mg/lb (8 mg/kg) may be administered if response to therapy is not complete.

Limitations
Cats
Indication

For the treatment of skin infections (wounds and abscesses) in cats caused by susceptible strains of Pasteurella multocida.

Dosage

Administer 3.6 mg/lb (8 mg/kg) body weight as a single, one-time subcutaneous injection.

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: Dog, No Use Class Stated Or Implied • Cat, No Use Class Stated Or Implied
Composition / specifications
Each milliliter of constituted solution contains 80 milligrams cefovecin as the sodium salt.
Cats
Indication
For the treatment of skin infections (wounds and abscesses) in cats caused by susceptible strains of Pasteurella multocida.
Dosage
Administer 3.6 mg/lb (8 mg/kg) body weight as a single, one-time subcutaneous injection.
Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian. For subcutaneous use in dogs and cats only.
Dogs
Indication
For the treatment of skin infections (secondary superficial pyoderma, abscesses, and wounds) in dogs caused by susceptible strains of Staphylococcus intermedius and Streptococcus canis (Group G).
Dosage
Administer 3.6 mg/lb (8 mg/kg) body weight as a single subcutaneous injection. A second subcutaneous injection of 3.6 mg/lb (8 mg/kg) may be administered if response to therapy is not complete.
Limitations
Federal law restricts this drug to use by or on the order of a licensed veterinarian. Maximum treatment should not exceed 2 injections. For subcutaneous use in dogs and cats only.

FDA page: Open in Animal Drugs @ FDA

Official Documents (FDA)

Direct links to FDA-hosted PDFs and SPL packages (when available).

Documents
  • Summary

    Dogs: For the treatment of skin infections (secondary superficial pyoderma, abscesses, and wounds) in dogs caused by susceptible strains of Staphylococcus intermedius and Streptococcus canis (Group G).

    Cats: For the treatment of skin infections (wounds and abscesses) in cats caused by susceptible strains of Pasteurella multocida.

SPL Packages

FDA page: Open in Animal Drugs @ FDA

Documents
  • Summary
    For the treatment of skin infections (wounds and abscesses) in cats caused by susceptible strains of Pasteurella multocida.
SPL Packages

FDA page: Open in Animal Drugs @ FDA

Usage

For the treatment of skin infections (wounds and abscesses) in cats caused by susceptible strains of Pasteurella multocida . For the treatment of skin infections (secondary superficial pyoderma, abscesses, and wounds) in dogs caused by susceptible strains of Staphylococcus intermedius and Streptococcus canis (Group G).

Source: FDA Animal Drugs @ FDA • Reference

Contraindications

Federal law restricts this drug to use by or on the order of a licensed veterinarian. For subcutaneous use in dogs and cats only. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Maximum treatment should not exceed 2 injections. For subcutaneous use in dogs and cats only.

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) • Cat Diarrhea (1) • Dog Decreased appetite (1) • Cat

Showing top 5 for Digestive.

Skin & allergy
Hives (1) • Dog Facial swelling (possible allergy) (1) • Dog

Showing top 5 for Skin & allergy.

Neurologic
Unsteady walking (1) • Cat Tiredness (1) • Dog

Showing top 5 for Neurologic.

Effectiveness
Lack of efficacy - NOS (1) • Dog

Showing top 5 for Effectiveness.

Other
Low blood pressure (1) • Dog Local erythema (1) • Dog Ketosis (1) • Cat Jaundice (1) • Dog Intentional misuse (1) • Cat
Show more (19)
Hypothermia (1) • Cat Hypokalaemia (1) • Dog Hyperpigmentation (1) • Dog Hiding (1) • Cat Gum disorder NOS (1) • Cat Glomerulonephritis (1) • Dog Elevated temperature (1) • Cat Dysphoria (1) • Cat Drinking a lot (1) • Dog Discomfort NOS (1) • Dog Delayed healing (1) • Dog Delayed fracture union (1) • Dog Decreased percentage of reticulocytes (1) • Dog Death by euthanasia (1) • Dog Death (1) • Dog Autoimmune disorder NOS (1) • Dog Anaphylactic-type reaction (1) • Dog Abnormal radiograph finding (1) • Cat Abnormal cytology (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.

Cat, Domestic Shorthair, Female, 18 year, 2.51 kilogram • Drug: MSK, Unknown • Reactions: Not sleeping, Dysphoria • Outcome: Outcome Unknown

  • Report ID: USA-USFDACVM-2025-US-056122
  • Serious AE: No
  • Treated For AE: No
  • Sex: Female
  • Age: 18.00 Year
  • Weight: 2.510 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Unknown
Reactions Reported:
Not sleeping Dysphoria
Outcomes: Outcome Unknown

Cat, Domestic Shorthair, Male, 6 year, 6.35 kilogram • Drug: MSK, Unknown • Reactions: Elevated temperature, Decreased appetite, Weight loss, Gum disorder NOS • Outcome: Ongoing

  • Report ID: USA-USFDACVM-2025-US-055975
  • Serious AE: No
  • Treated For AE: No
  • Sex: Male
  • Age: 6.00 Year
  • Weight: 6.350 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Unknown
Reactions Reported:
Elevated temperature Decreased appetite Weight loss Gum disorder NOS
Outcomes: Ongoing

Cat, Domestic Mediumhair, Female, 13 year, 2.858 kilogram • Drug: MSK, Subcutaneous, Dose: 0.30 mL per animal • Reactions: Tiredness (lethargy), Unresponsive to stimuli, Not eating, Not drinking, Hiding… • Outcome: Ongoing

  • Report ID: USA-USFDACVM-2025-US-055801
  • Serious AE: No
  • Treated For AE: Yes
  • Sex: Female
  • Age: 13.00 Year
  • Weight: 2.858 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Subcutaneous
  • Dose: 0.30 mL per animal
Reactions Reported:
Tiredness (lethargy) Unresponsive to stimuli Not eating Not drinking Hiding Unsteady walking (ataxia) Abnormal radiograph finding Hypothermia Tympanic opacity Weight loss Malaise Muscle weakness NOS Intentional misuse Lack of efficacy - NOS
Outcomes: Ongoing

Cat, Cat (unknown), Female, 12 year, 3.44 kilogram • Drug: MSK, Unknown • Reactions: Tiredness (lethargy), Loss of appetite • Outcome: Ongoing

  • Report ID: USA-USFDACVM-2025-US-055698
  • Serious AE: No
  • Treated For AE: No
  • Sex: Female
  • Age: 12.00 Year
  • Weight: 3.440 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Unknown
Reactions Reported:
Tiredness (lethargy) Loss of appetite
Outcomes: Ongoing

Cat, Domestic Mediumhair, Female, 16 year, 4.5 kilogram • Drug: MSK, Unknown • Reactions: Ketosis • Outcome: Outcome Unknown

  • Report ID: USA-USFDACVM-2025-US-054426
  • Serious AE: No
  • Treated For AE: No
  • Sex: Female
  • Age: 16.00 Year
  • Weight: 4.500 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Unknown
Reactions Reported:
Ketosis
Outcomes: Outcome Unknown

Dog, Terrier - Yorkshire, Male, 8 year, 3.629 kilogram • Drug: MSK, Injection, Subcutaneous, Dose: 32 Milligram per dose, Frequency: 1 per day • Reactions: Jaundice, Low blood urea nitrogen, Low creatinine, Hypokalaemia, Death by euthanasia • Outcome: Euthanized

  • Report ID: USA-USFDACVM-2025-US-053982
  • Serious AE: Yes
  • Treated For AE: Yes
  • Sex: Male
  • Age: 8.00 Year
  • Weight: 3.629 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Subcutaneous
  • Form: Injection
  • Dose: 32 Milligram per dose
  • Frequency: 1 per day
Reactions Reported:
Jaundice Low blood urea nitrogen Low creatinine Hypokalaemia Death by euthanasia
Outcomes: Euthanized

Dog, Crossbred Canine/dog, Female, 12 year, 10.886 kilogram • Drug: MSK, Unknown • Reactions: Vomiting, Discomfort NOS, Not sleeping, Whining, Not eating… • Outcome: Ongoing

  • Report ID: USA-USFDACVM-2025-US-051294
  • Serious AE: No
  • Treated For AE: No
  • Sex: Female
  • Age: 12.00 Year
  • Weight: 10.886 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Unknown
Reactions Reported:
Vomiting Discomfort NOS Not sleeping Whining Not eating Diarrhea Tiredness (lethargy)
Outcomes: Ongoing

Dog, Poodle - Toy, Male, 4.5 year, 4.54 kilogram • Drug: MSK, Unknown • Reactions: Polyuria, Urinary incontinence • Outcome: Outcome Unknown

  • Report ID: USA-USFDACVM-2025-US-048414
  • Serious AE: No
  • Treated For AE: No
  • Sex: Male
  • Age: 4.50 Year
  • Weight: 4.540 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Unknown
Reactions Reported:
Polyuria Urinary incontinence
Outcomes: Outcome Unknown

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.

Share Your Thoughts

Let others know your experience or advice regarding this medication.

This medication has not been reviewed by a veterinarian yet.