United States · FDA National Drug Code directory
Amoxicillin
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
- 60687-798_4ee4fb77-9fd6-ea5e-e063-6394a90a0d9c
- Product NDC
- 60687-798
- Form
- TABLET, FILM COATED
- Composition / generic term
- Amoxicillin
- Labeler
- American Health Packaging
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250325 / 20261231
Source-listed ingredients
- AMOXICILLIN — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 BLISTER PACK in 1 CARTON (60687-798-25) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-798-95) · 60687-798-25
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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