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
- 43602-602_a2adad08-283e-4617-b3db-1eade7f5b296
- Product NDC
- 43602-602
- Form
- TABLET
- Composition / generic term
- Famotidine
- Labeler
- Ascent Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20211103
- Source listing expiry
- 20261231
Source-listed ingredients
- FAMOTIDINE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (43602-602-03) / 300 TABLET in 1 BOTTLE · 43602-602-03
- 1 BOTTLE in 1 CARTON (43602-602-30) / 30 TABLET in 1 BOTTLE · 43602-602-30
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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