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
- 10267-5690_1c656b34-6eeb-cc3f-e063-6294a90ad3f8
- Product NDC
- 10267-5690
- Form
- TABLET, COATED
- Composition / generic term
- Famotidine
- Labeler
- Contract Pharmacal Corp.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240831
- Source listing expiry
- 20261231
Source-listed ingredients
- FAMOTIDINE — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, COATED in 1 BOTTLE (10267-5690-1) · 10267-5690-1
- 1000 TABLET, COATED in 1 BOTTLE (10267-5690-4) · 10267-5690-4
- 500 TABLET, COATED in 1 BOTTLE (10267-5690-5) · 10267-5690-5
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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