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
- 82804-134_c8e5ad7d-09b7-41d9-8cb0-467b3e8df74f
- Product NDC
- 82804-134
- Form
- POWDER, FOR SUSPENSION
- Composition / generic term
- Amoxicillin
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140915
- Source listing expiry
- 20261231
Source-listed ingredients
- AMOXICILLIN — 250 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 150 mL in 1 BOTTLE (82804-134-15) · 82804-134-15
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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