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
- 0781-1852_6a6233c9-2bba-4d8c-9bfa-e5c5055cf91f
- Product NDC
- 0781-1852
- Form
- TABLET, FILM COATED
- Composition / generic term
- Amoxicillin and Clavulanate Potassium
- Labeler
- Sandoz Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20020314
- Source listing expiry
- 20261231
Source-listed ingredients
- AMOXICILLIN — 875 mg/1
- CLAVULANATE POTASSIUM — 125 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (0781-1852-01) · 0781-1852-01
- 100 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (0781-1852-13) · 0781-1852-13
- 20 TABLET, FILM COATED in 1 BOTTLE (0781-1852-20) · 0781-1852-20
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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