United States · FDA National Drug Code directory
Famotidine
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
- 0338-5197_bb9e28a8-1076-4c48-9a19-cc43bcd64862
- Product NDC
- 0338-5197
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Famotidine
- Labeler
- Baxter Healthcare Corporation
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20010510
- Source listing expiry
- 20271231
Source-listed ingredients
- FAMOTIDINE — 20 mg/50mL
These values do not establish equivalence or a dose recommendation.
Packages
- 12 BAG in 1 CARTON (0338-5197-41) / 50 mL in 1 BAG · 0338-5197-41
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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