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
- 0172-5729_c1d3bda6-9457-4b20-b660-0a62f52eb36a
- Product NDC
- 0172-5729
- Form
- TABLET, FILM COATED
- Composition / generic term
- Famotidine
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20010416
- Source listing expiry
- 20271231
Source-listed ingredients
- FAMOTIDINE — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (0172-5729-60) · 0172-5729-60
- 500 TABLET, FILM COATED in 1 BOTTLE (0172-5729-70) · 0172-5729-70
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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