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
- 76420-871_26377eb9-ab0a-505d-e063-6394a90af5db
- Product NDC
- 76420-871
- Form
- CAPSULE
- Composition / generic term
- Amoxicillin
- Labeler
- Asclemed USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20171212
- Source listing expiry
- 20261231
Source-listed ingredients
- AMOXICILLIN — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 21 CAPSULE in 1 BOTTLE, PLASTIC (76420-871-03) · 76420-871-03
- 30 CAPSULE in 1 BLISTER PACK (76420-871-05) · 76420-871-05
- 21 CAPSULE in 1 BLISTER PACK (76420-871-06) · 76420-871-06
- 28 CAPSULE in 1 BLISTER PACK (76420-871-07) · 76420-871-07
- 30 CAPSULE in 1 BOTTLE, PLASTIC (76420-871-08) · 76420-871-08
- 20 CAPSULE in 1 BOTTLE, PLASTIC (76420-871-09) · 76420-871-09
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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