United States · FDA National Drug Code directory
berkley and jensen 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
- 68391-300_8459c675-5144-445c-afdb-c09b445fc14b
- Product NDC
- 68391-300
- Form
- TABLET, FILM COATED
- Composition / generic term
- Famotidine
- Labeler
- BJWC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20131209
- Source listing expiry
- 20271231
Source-listed ingredients
- FAMOTIDINE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 BOTTLE in 1 PACKAGE (68391-300-82) / 100 TABLET, FILM COATED in 1 BOTTLE · 68391-300-82
- 2 BOTTLE in 1 PACKAGE (68391-300-85) / 125 TABLET, FILM COATED in 1 BOTTLE (68391-300-05) · 68391-300-85
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 →