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
- 0143-9982_29e9e32b-e9a3-48b5-a1c7-14b3bbe447e5
- Product NDC
- 0143-9982
- Form
- POWDER, FOR SUSPENSION
- Composition / generic term
- Amoxicillin and Clavulanate Potassium
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20071201
- Source listing expiry
- 20271231
Source-listed ingredients
- AMOXICILLIN — 400 mg/5mL
- CLAVULANIC ACID — 57 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 100 mL in 1 BOTTLE (0143-9982-01) · 0143-9982-01
- 50 mL in 1 BOTTLE (0143-9982-50) · 0143-9982-50
- 75 mL in 1 BOTTLE (0143-9982-75) · 0143-9982-75
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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