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
- 69230-326_eabd2ff8-a7d9-2ac4-e053-2995a90a3b40
- Product NDC
- 69230-326
- Form
- TABLET, FILM COATED
- Composition / generic term
- famotidine
- Labeler
- Camber Consumer Care Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20211108
- Source listing expiry
- 20261231
Source-listed ingredients
- FAMOTIDINE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (69230-326-01) / 100 TABLET, FILM COATED in 1 BOTTLE · 69230-326-01
- 1 BOTTLE in 1 CARTON (69230-326-05) / 500 TABLET, FILM COATED in 1 BOTTLE · 69230-326-05
- 1 BOTTLE in 1 CARTON (69230-326-10) / 1000 TABLET, FILM COATED in 1 BOTTLE · 69230-326-10
- 1 BOTTLE in 1 CARTON (69230-326-30) / 30 TABLET, FILM COATED in 1 BOTTLE · 69230-326-30
- 1 BOTTLE in 1 CARTON (69230-326-60) / 60 TABLET, FILM COATED in 1 BOTTLE · 69230-326-60
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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