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
- 73043-010_e5eda5f6-317c-43ac-b1d7-c6ce635593da
- Product NDC
- 73043-010
- Form
- POWDER, FOR SUSPENSION
- Composition / generic term
- amoxicillin and clavulanate potassium
- Labeler
- Devatis, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240705
- Source listing expiry
- 20261231
Source-listed ingredients
- AMOXICILLIN — 250 mg/5mL
- CLAVULANATE POTASSIUM — 62.5 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 75 mL in 1 BOTTLE (73043-010-01) · 73043-010-01
- 100 mL in 1 BOTTLE (73043-010-02) · 73043-010-02
- 150 mL in 1 BOTTLE (73043-010-03) · 73043-010-03
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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