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
51316-816_35e8d139-0f84-4c0e-b43b-bf28f8d9f28e
Product NDC
51316-816
Form
TABLET, FILM COATED
Composition / generic term
Famotidine
Labeler
CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
Marketing category
ANDA
Marketing start / end (source format)
20260803
Source listing expiry
20271231

Source-listed ingredients

  • FAMOTIDINE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (51316-816-39) / 30 TABLET, FILM COATED in 1 BOTTLE · 51316-816-39

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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