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
- 63187-729_8407c6b1-788b-479e-8c41-3d6fe2b7b8ec
- Product NDC
- 63187-729
- Form
- TABLET, FILM COATED
- Composition / generic term
- Amoxicillin
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20051109
- Source listing expiry
- 20261231
Source-listed ingredients
- AMOXICILLIN — 875 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 14 TABLET, FILM COATED in 1 BOTTLE (63187-729-14) · 63187-729-14
- 20 TABLET, FILM COATED in 1 BOTTLE (63187-729-20) · 63187-729-20
- 21 TABLET, FILM COATED in 1 BOTTLE (63187-729-21) · 63187-729-21
- 28 TABLET, FILM COATED in 1 BOTTLE (63187-729-28) · 63187-729-28
- 30 TABLET, FILM COATED in 1 BOTTLE (63187-729-30) · 63187-729-30
- 40 TABLET, FILM COATED in 1 BOTTLE (63187-729-40) · 63187-729-40
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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