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
- 62135-095_57477f96-ff03-67dc-e063-6294a90ad89d
- Product NDC
- 62135-095
- Form
- POWDER, FOR SUSPENSION
- Composition / generic term
- amoxicillin and clavulanate potassium
- Labeler
- Chartwell RX, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20040923
- Source listing expiry
- 20271231
Source-listed ingredients
- AMOXICILLIN — 600 mg/5mL
- CLAVULANATE POTASSIUM — 42.9 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 125 mL in 1 BOTTLE (62135-095-13) · 62135-095-13
- 200 mL in 1 BOTTLE (62135-095-22) · 62135-095-22
- 75 mL in 1 BOTTLE (62135-095-75) · 62135-095-75
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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