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
- 81964-220_52498ef2-86fc-72b6-e063-6294a90a4232
- Product NDC
- 81964-220
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- amoxicillin and clavulanate potassium
- Labeler
- USAntibiotics, LLC
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20251215
- Source listing expiry
- 20271231
Source-listed ingredients
- AMOXICILLIN — 562.5 mg/1
- CLAVULANATE POTASSIUM — 62.5 mg/1
- AMOXICILLIN SODIUM — 437.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (81964-220-28) · 81964-220-28
- 40 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (81964-220-40) · 81964-220-40
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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