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
- 69842-087_1180f756-b6a5-4bc8-a16d-f54945aa6232
- Product NDC
- 69842-087
- Form
- TABLET, FILM COATED
- Composition / generic term
- Famotidine
- Labeler
- CVS Pharmacy, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200203
- 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 (69842-087-14) / 50 TABLET, FILM COATED in 1 BOTTLE · 69842-087-14
- 1 BOTTLE in 1 CARTON (69842-087-21) / 100 TABLET, FILM COATED in 1 BOTTLE · 69842-087-21
- 1 BOTTLE in 1 CARTON (69842-087-53) / 25 TABLET, FILM COATED in 1 BOTTLE · 69842-087-53
- 1 BLISTER PACK in 1 CARTON (69842-087-79) / 8 TABLET, FILM COATED in 1 BLISTER PACK · 69842-087-79
- 2 BOTTLE in 1 CARTON (69842-087-80) / 100 TABLET, FILM COATED in 1 BOTTLE · 69842-087-80
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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