United States · FDA National Drug Code directory
Amoxicillin and Clavulanate Potassium
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0093-2274_aaf9ce2f-41c3-489c-b5c1-f4f553d84854
- Product NDC
- 0093-2274
- Form
- TABLET, FILM COATED
- Composition / generic term
- Amoxicillin and Clavulanate Potassium
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20021031
- Source listing expiry
- 20261231
Source-listed ingredients
- AMOXICILLIN — 500 mg/1
- CLAVULANATE POTASSIUM — 125 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 TABLET, FILM COATED in 1 BOTTLE (0093-2274-34) · 0093-2274-34
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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