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
- 0781-6039_f4681ad2-fcc2-41f6-9100-90fb4524cd28
- Product NDC
- 0781-6039
- Form
- POWDER, FOR SUSPENSION
- Composition / generic term
- Amoxicillin
- Labeler
- Sandoz Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070326
- Source listing expiry
- 20271231
Source-listed ingredients
- AMOXICILLIN — 125 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 100 mL in 1 BOTTLE (0781-6039-46) · 0781-6039-46
- 150 mL in 1 BOTTLE (0781-6039-55) · 0781-6039-55
- 80 mL in 1 BOTTLE (0781-6039-58) · 0781-6039-58
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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