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
- 69230-327_eabd2ff8-a7d9-2ac4-e053-2995a90a3b40
- Product NDC
- 69230-327
- 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 — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (69230-327-01) / 100 TABLET, FILM COATED in 1 BOTTLE · 69230-327-01
- 1 BOTTLE in 1 CARTON (69230-327-05) / 500 TABLET, FILM COATED in 1 BOTTLE · 69230-327-05
- 1 BOTTLE in 1 CARTON (69230-327-10) / 1000 TABLET, FILM COATED in 1 BOTTLE · 69230-327-10
- 1 BOTTLE in 1 CARTON (69230-327-30) / 30 TABLET, FILM COATED in 1 BOTTLE · 69230-327-30
- 1 BOTTLE in 1 CARTON (69230-327-50) / 50 TABLET, FILM COATED in 1 BOTTLE · 69230-327-50
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →