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
- 68788-4179_2c7a4de8-002a-472c-90d8-4c39a1f188c3
- Product NDC
- 68788-4179
- Form
- POWDER, FOR SUSPENSION
- Composition / generic term
- Amoxicillin and Clavulanate Potassium
- Labeler
- Preferred Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260731
- 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 (68788-4179-1) · 68788-4179-1
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 →