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
- 85534-0072_55af4d00-f2af-456b-e063-6394a90a75e5
- Product NDC
- 85534-0072
- Form
- POWDER, FOR SUSPENSION
- Composition / generic term
- Amoxicillin
- Labeler
- HAWAII REPACK, INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070326
- Source listing expiry
- 20271231
Source-listed ingredients
- AMOXICILLIN — 250 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 80 mL in 1 BOTTLE (85534-0072-0) · 85534-0072-0
- 100 mL in 1 BOTTLE (85534-0072-1) · 85534-0072-1
- 150 mL in 1 BOTTLE (85534-0072-2) · 85534-0072-2
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →