Roxee Meds Catalog
Clavulanate Potassium
Medication catalog facts with explicit FDA-approval, off-label, source-limited, and safety context.
Veterinary professional?
Data freshness
Roxee is still reviewing source support for this medication profile.
Roxee has safety or ingredient evidence for this medication, but a regulatory product/application match is still pending.
openFDA reaction terms and case summaries are supporting evidence, not proof of causality.
Source timing details
-
Storefront facts:
Source Roxee
| Refreshed May 2, 2026, 10:05 AM UTC
The storefront fact projection used for browse cards and quick facts.
Evidence
Reviewed / Updated / Sources
Reviewed by: Not available
Last reviewed: May 2, 2026
Updated: May 2, 2026, 10:05 AM UTC
- Medication contraindications · safety_warning
- openFDA case USA-USFDACVM-2025-US-075506 · adverse_reaction
- FOI summary · document
- FOI summary · document
- FOI summary · document
Clavulanate Potassium
Drug type: Generic ingredient • Generic profile • Regulatory linkage incomplete
Species: Both
Approval status: Official document linked, regulatory match incomplete. An official source document is available, but Roxee has not linked this row to a confirmed FDA animal-drug application or product record yet.
Medication Snapshot
Merged from the current Roxee medication system with field-level provenance, freshness, and completeness tracking.
Clavulanate Potassium
Clavamox Drops are indicated in the treatment of skin and soft tissue infections such as wounds, abscesses, cellulitis, superficial/juvenile and deep pyoderma due to susceptible strains of the following organisms: ß-lactamase-producing Staphylo coccus aureus , non- ß -lactamase-producing Staphylococcus aureus , Staphylococcus spp., Streptococcus spp., and E. coli . Periodontal infections due to susceptible strains of both aerobic and anaerobic bacteria. Clavamox has been shown to be clinically effective for treating cases of canine periodontal disease. Clavamox Drops are indicated in the treatment of skin and soft tissue infections such as wounds, abscesses, and cellulitis/dermatitis due to susceptible strains of the following organisms: ß-lactamase-producing Staphylococcus aureus , non-ß-lactamase-producing Staphylococcus aureus , Staphylococcus spp., Streptococcus spp., E. coli , Pasteurella multocida , and Pasteurella spp. Urinary tract infections (cystitis) due to susceptible strains of E. coli . Therapy may be initiated with Clavamox prior to obtaining results from bacteriological and susceptibility studies. A culture should be obtained prior to treatment to determine susceptibility of the organisms to Clavamox. Following determination of susceptibility results and clinical response to medication, therapy may be reevaluated. For the treatment of skin and soft tissue infections such as wounds, abscesses, and cellulitis/dermatitis due to susceptible strains of the following organisms: ß-lactamase-producing Staphylococcus aureus, non-ß-lactamase-producing Staphylococcus aureus, Staphylococcus spp., Streptococcus spp., E. coli, and Pasteurella spp. Urinary tract infections (cystitis) due to susceptible strains of E. coli. Species commonly shown: Both.
Indications / Uses
Clavamox Drops are indicated in the treatment of skin and soft tissue infections such as wounds, abscesses, cellulitis, superficial/juvenile and deep pyoderma due to susceptible strains of the following organisms: ß-lactamase-producing Staphylo coccus aureus , non- ß -lactamase-producing Staphylococcus aureus , Staphylococcus spp., Streptococcus spp., and E. coli . Periodontal infections due to susceptible strains of both aerobic and anaerobic bacteria. Clavamox has been shown to be clinically effective for treating cases of canine periodontal disease. Clavamox Drops are indicated in the treatment of skin and soft tissue infections such as wounds, abscesses, and cellulitis/dermatitis due to susceptible strains of the following organisms: ß-lactamase-producing Staphylococcus aureus , non-ß-lactamase-producing Staphylococcus aureus , Staphylococcus spp., Streptococcus spp., E. coli , Pasteurella multocida , and Pasteurella spp. Urinary tract infections (cystitis) due to susceptible strains of E. coli . Therapy may be initiated with Clavamox prior to obtaining results from bacteriological and susceptibility studies. A culture should be obtained prior to treatment to determine susceptibility of the organisms to Clavamox. Following determination of susceptibility results and clinical response to medication, therapy may be reevaluated. For the treatment of skin and soft tissue infections such as wounds, abscesses, and cellulitis/dermatitis due to susceptible strains of the following organisms: ß-lactamase-producing Staphylococcus aureus, non-ß-lactamase-producing Staphylococcus aureus, Staphylococcus spp., Streptococcus spp., E. coli, and Pasteurella spp. Urinary tract infections (cystitis) due to susceptible strains of E. coli.
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.
Side Effects
Top reported reactions (openFDA): Elevated alanine aminotransferase (ALT), Brain disorder NOS, Bruising, Circling - neurological disorder (see also Behavioural disorders), Distension of abdomen, Ecchymosis.
FAQ
Related Conditions
Source Transparency
- Verified source: https://www.roxee.ai/meds/
- Verified source: https://animaldrugsatfda.fda.gov
- Verified source: https://api.fda.gov/animalandveterinary/event.json
- Verified source: https://www.roxee.ai/conditions/
- Verified source: https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/1953
- Verified source: https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/11187
- Last refreshed: May 2, 2026, 10:05 a.m.
- Validation status: Incomplete
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Start here first for the safest next-step summary before the deeper medication detail.
Used for:
Clavamox Drops are indicated in the treatment of skin and soft tissue infections such as wounds, abscesses, cellulitis, superficial/juvenile and deep pyoderma due to susceptible strains of the following organisms: ß-lact...
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:
- wobbly/unsteady walking (1 reports)
- Pain NOS (1 reports)
- Pacing (1 reports)
When to call the vet:
- Repeated vomiting or diarrhea.
- Severe lethargy (hard to wake, very low energy).
- Collapse or fainting.
- Trouble breathing.
- Facial swelling or hives.
- Blood in vomit or stool.
Regulatory restrictions are shown in Vet View.
What to tell or ask your vet today:
- Is this medicine the right fit for my pet’s current symptoms?
- Which warning signs mean I should call back right away?
- How should I handle missed doses or refusal to take the medicine?
Major cautions & emergency warning signs
Side effects to monitor:
- wobbly/unsteady walking
- Pain NOS
- Pacing
Most reported reactions:
- Unsteady walking (ataxia) (1 reports)
- Pain NOS (1 reports)
- Pacing (1 reports)
Emergency warning signs:
- Repeated vomiting or diarrhea.
- Severe lethargy (hard to wake, very low energy).
- Collapse or fainting.
- Trouble breathing.
Quick Facts
Official label facts first, then secondary summaries. Marketing content is separated below.
Warnings / Contraindications
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.
- https://animaldrugsatfda.fda.gov · safety_warning · Medication contraindications
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.
Grouped by Body System
Most Reported Reactions
| Reaction | Body system | Cases | Species | Serious cases |
|---|---|---|---|---|
| Neurologic | 1 | Cat | 1 | |
| Other | 1 | Dog | 1 | |
| Other | 1 | Dog | 1 | |
| Other | 1 | Dog | 1 | |
| Other | 1 | Dog | 1 | |
| Other | 1 | Cat | 1 | |
| Other | 1 | Dog | 1 | |
| Other | 1 | Dog | 1 |
Species coverage: Dog (22) Cat (10)
View detailed reaction table
| Reaction | Body system | Species | Seriousness | Frequency | Reports |
|---|---|---|---|---|---|
| Neurologic | Cat | Serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Other | Cat | Non-serious | - | 1 | |
| Other | 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 | Serious | - | 1 | |
| Other | Cat | Serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Other | Cat | Serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Other | 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 | |
| Other | Dog | Serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Digestive | Cat | Non-serious | - | 1 | |
| Other | Cat | Non-serious | - | 1 | |
| Neurologic | Dog | Serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Other | Cat | Non-serious | - | 1 |
- https://api.fda.gov/animalandveterinary/event.json · adverse_reaction · openFDA case USA-USFDACVM-2025-US-075506
Documents
Owner handouts and official technical documents open on-page first, with the original source still one click away.
Owner handouts
0Official label / PI
0SPL
0FOI
5FOI Summary oA 200-709 Approved August 18, 2021.pdf
FOI · FOI summary
FOI Summary oA 200-702 Approved April 23, 2021.pdf
FOI · FOI summary
N055101_Supp_12_23_1997.pdf
FOI · FOI summary
FOI Summary oA 200-604 Approved October 20, 2021.pdf
FOI · FOI summary
UCM524262.pdf
FOI · FOI summary
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/11187 · document · FOI summary
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/10753 · document · FOI summary
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/1953 · document · FOI summary
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/11403 · document · FOI summary
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/1263 · document · FOI summary
Veterinary reference (advanced)
Canonical medication sections are above. This legacy block remains available for deeper cross-reference without cluttering the primary workflow.
At a Glance
Quick facts and links to official labeling and safety signals.
-
Storefront facts:
Source Roxee
| Refreshed May 2, 2026, 10:05 AM UTC
The storefront fact projection used for browse cards and quick facts.
Counseling and Monitoring Highlights
Global Pet owner/Vet mode is controlled in the header. This section avoids duplicate in-page persona tabs.
- Federal law restricts this drug to use by or on the order of a licensed veterinarian. (Contraindication, High)
Identifiers & Packages
Normalized identifiers (NDC/NADA/ANADA) and package metadata from regulator listings.
| Package NDC | Product NDC | Form / Route | Status |
|---|---|---|---|
| 11695-6991-1 | 11695 | - | |
| 11695-6992-1 | 11695 | - | |
| 11695-6993-1 | 11695 | - | |
| 11695-6994-1 | 11695 | - | |
| 11695-7007-1 | 11695 | - | |
| 13744-540-01 | 13744 | - | |
| 13744-541-01 | 13744 | - | |
| 13744-542-01 | 13744 | - | |
| 13744-543-01 | 13744 | - | |
| 17033-440-07 | 17033 | - | |
| 17033-440-21 | 17033 | - | |
| 17033-441-07 | 17033 | - | |
| 17033-441-21 | 17033 | - | |
| 17033-442-07 | 17033 | - | |
| 17033-442-21 | 17033 | - | |
| 17033-443-07 | 17033 | - | |
| 17033-443-21 | 17033 | - | |
| 17033-451-15 | 17033 | - | |
| 46066-087-17 | 46066 | - | |
| 46066-111-60 | 46066 | - |
Enriched Documents
Documents are tiered by source trust: Official, Clinical, Manufacturer, Marketing.
-
FOI Summary oA 200-709 Approved August 18, 2021.pdf
• FOI summary • Official
• April 10, 2024
FDA FOI summary for application 200709
-
FOI Summary oA 200-702 Approved April 23, 2021.pdf
• FOI summary • Official
• Dec. 12, 2023
FDA FOI summary for application 200702
-
N055101_Supp_12_23_1997.pdf
• FOI summary • Official
• Jan. 12, 2023
FDA FOI summary for application 55101
-
FOI Summary oA 200-604 Approved October 20, 2021.pdf
• FOI summary • Official
• July 25, 2022
FDA FOI summary for application 200604
-
UCM524262.pdf
• FOI summary • Official
• March 29, 2022
FDA FOI summary for application 200592
Data Sources & Change Log
Every non-trivial field is expected to include provenance and update timestamps.
- contraindications: Federal law restricts this drug to use by or on the order of a licensed veterinarian. (Clinical, 2026-05-02)
- contraindications: Federal law restricts this drug to use by or on the order of a licensed veterinarian. (Clinical, 2026-04-15)
- contraindications: Federal law restricts this drug to use by or on the order of a licensed veterinarian. (Clinical, 2026-04-11)
- side_effects: Top reported reactions (openFDA): Elevated alanine aminotransferase (ALT), Brain disorder NOS, Bruising, Circling - neurological disorder (see also Behavioural… (Clinical, 2026-05-02)
- side_effects: Top reported reactions (openFDA): Elevated alanine aminotransferase (ALT), Brain disorder NOS, Bruising, Circling - neurological disorder (see also Behavioural… (Clinical, 2026-04-15)
- side_effects: Top reported reactions (openFDA): Elevated alanine aminotransferase (ALT), Brain disorder NOS, Bruising, Circling - neurological disorder (see also Behavioural… (Clinical, 2026-04-11)
- usage: Clavamox Drops are indicated in the treatment of skin and soft tissue infections such as wounds, abscesses, cellulitis, superficial/juvenile and deep pyoderma … (Clinical, 2026-05-02)
- usage: Clavamox Drops are indicated in the treatment of skin and soft tissue infections such as wounds, abscesses, cellulitis, superficial/juvenile and deep pyoderma … (Clinical, 2026-04-15)
- usage: Clavamox Drops are indicated in the treatment of skin and soft tissue infections such as wounds, abscesses, cellulitis, superficial/juvenile and deep pyoderma … (Clinical, 2026-04-11)
- contraindications: Federal law restricts this drug to use by or on the order of a licensed veterinarian. (Official, 2026-04-30)
- contraindications: Federal law restricts this drug to use by or on the order of a licensed veterinarian. (Official, 2026-02-12)
- side_effects: Top reported reactions (openFDA): Elevated alanine aminotransferase (ALT), Brain disorder NOS, Bruising, Circling - neurological disorder (see also Behavioural… (Official, 2026-04-30)
- side_effects: Top reported reactions (openFDA): Elevated alanine aminotransferase (ALT), Brain disorder NOS, Bruising, Circling - neurological disorder (see also Behavioural… (Official, 2026-02-12)
- usage: Clavamox Drops are indicated in the treatment of skin and soft tissue infections such as wounds, abscesses, cellulitis, superficial/juvenile and deep pyoderma … (Official, 2026-04-30)
- usage: Clavamox Drops are indicated in the treatment of skin and soft tissue infections such as wounds, abscesses, cellulitis, superficial/juvenile and deep pyoderma … (Official, 2026-02-12)
- side_effects updated 2026-05-02 10:05 by etl_backfill • Backfilled from existing medication fields
- contraindications updated 2026-05-02 10:05 by etl_backfill • Backfilled from existing medication fields
- usage updated 2026-05-02 10:05 by etl_backfill • Backfilled from existing medication fields
- side_effects updated 2026-04-30 10:09 by etl_backfill • Backfilled from existing medication fields
- contraindications updated 2026-04-30 10:09 by etl_backfill • Backfilled from existing medication fields
- usage updated 2026-04-30 10:09 by etl_backfill • Backfilled from existing medication fields
- side_effects updated 2026-04-15 10:04 by etl_backfill • Backfilled from existing medication fields
- contraindications updated 2026-04-15 10:04 by etl_backfill • Backfilled from existing medication fields
- usage updated 2026-04-15 10:04 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
Usage
Clavamox Drops are indicated in the treatment of skin and soft tissue infections such as wounds, abscesses, cellulitis, superficial/juvenile and deep pyoderma due to susceptible strains of the following organisms: ß-lactamase-producing Staphylo coccus aureus , non- ß -lactamase-producing Staphylococcus aureus , Staphylococcus spp., Streptococcus spp., and E. coli . Periodontal infections due to susceptible strains of both aerobic and anaerobic bacteria. Clavamox has been shown to be clinically effective for treating cases of canine periodontal disease. Clavamox Drops are indicated in the treatment of skin and soft tissue infections such as wounds, abscesses, and cellulitis/dermatitis due to susceptible strains of the following organisms: ß-lactamase-producing Staphylococcus aureus , non-ß-lactamase-producing Staphylococcus aureus , Staphylococcus spp., Streptococcus spp., E. coli , Pasteurella multocida , and Pasteurella spp. Urinary tract infections (cystitis) due to susceptible strains of E. coli . Therapy may be initiated with Clavamox prior to obtaining results from bacteriological and susceptibility studies. A culture should be obtained prior to treatment to determine susceptibility of the organisms to Clavamox. Following determination of susceptibility results and clinical response to medication, therapy may be reevaluated. For the treatment of skin and soft tissue infections such as wounds, abscesses, and cellulitis/dermatitis due to susceptible strains of the following organisms: ß-lactamase-producing Staphylococcus aureus, non-ß-lactamase-producing Staphylococcus aureus, Staphylococcus spp., Streptococcus spp., E. coli, and Pasteurella spp. Urinary tract infections (cystitis) due to susceptible strains of E. coli.
Contraindications
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).
Showing top 5 for Digestive.
Showing top 5 for Neurologic.
Show more (24)
Showing top 5 for Other.
Data source: FDA openFDA Animal & Veterinary adverse event reports.
Adverse Event Case Summaries (openFDA)
These are individual FDA adverse event reports. They are unverified and do not prove the medication caused the reaction.
No case-level openFDA reports are linked for this medication yet.
Data source: FDA openFDA Animal & Veterinary adverse event reports.
Overdose Information
No approved overdose-management text is linked yet. If overdose is suspected, contact a veterinarian or emergency clinic immediately.
Storage & Handling
No approved storage guidance is linked yet for this ingredient. Use manufacturer packaging and veterinary guidance for handling/storage.
Share Your Thoughts
Let others know your experience or advice regarding this medication.
This medication has not been reviewed by a veterinarian yet.