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
- 0143-9249_46aeb040-bd8f-4fcf-bfb7-98a8efc0a368
- Product NDC
- 0143-9249
- Form
- TABLET
- Composition / generic term
- Amoxicillin and Clavulanate Potassium
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160823
- 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 in 1 BOTTLE (0143-9249-20) · 0143-9249-20
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 →