United States · FDA National Drug Code directory
ACID REDUCER
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
- 51316-511_050a6f93-cc1d-40ae-af26-0ce8e40d5774
- Product NDC
- 51316-511
- Form
- TABLET, FILM COATED
- Composition / generic term
- Famotidine
- Labeler
- CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260413
- Source listing expiry
- 20271231
Source-listed ingredients
- FAMOTIDINE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (51316-511-63) / 25 TABLET, FILM COATED in 1 BOTTLE · 51316-511-63
- 1 BOTTLE in 1 CARTON (51316-511-71) / 50 TABLET, FILM COATED in 1 BOTTLE · 51316-511-71
- 1 BOTTLE in 1 CARTON (51316-511-78) / 100 TABLET, FILM COATED in 1 BOTTLE · 51316-511-78
- 1 BOTTLE in 1 CARTON (51316-511-98) / 75 TABLET, FILM COATED in 1 BOTTLE · 51316-511-98
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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