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
- 68788-8485_70b50c77-9a69-4898-bfe2-813872788a4e
- Product NDC
- 68788-8485
- Form
- TABLET, FILM COATED
- Composition / generic term
- FAMOTIDINE
- Labeler
- Preferred Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230718
- Source listing expiry
- 20271231
Source-listed ingredients
- FAMOTIDINE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (68788-8485-3) · 68788-8485-3
- 14 TABLET, FILM COATED in 1 BOTTLE (68788-8485-4) · 68788-8485-4
- 60 TABLET, FILM COATED in 1 BOTTLE (68788-8485-6) · 68788-8485-6
- 90 TABLET, FILM COATED in 1 BOTTLE (68788-8485-9) · 68788-8485-9
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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