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
- 73043-006_a51715ae-3a5c-4502-a9d9-a7469d5adc69
- Product NDC
- 73043-006
- Form
- TABLET, FILM COATED
- Composition / generic term
- amoxicillin and clavulanate potassium
- Labeler
- Devatis, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20241101
- 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
- 20 TABLET, FILM COATED in 1 BOTTLE (73043-006-20) · 73043-006-20
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →