NDC 51316-511 – Acid Reducer

Famotidine 20 mg/1 · Tablet, Film Coated · Oral

Human Otc Drug

Product NDC51316-511

Product details

Brand name
Acid Reducer
Generic name
Famotidine
Labeler
CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077351
Marketed since
April 13, 2026
Listing expires
December 31, 2027
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Acid Reducer →

Package NDC codes (4)

Package NDCDescriptionSince
51316-511-631 BOTTLE in 1 CARTON (51316-511-63) / 25 TABLET, FILM COATED in 1 BOTTLEApr 13, 2026
51316-511-711 BOTTLE in 1 CARTON (51316-511-71) / 50 TABLET, FILM COATED in 1 BOTTLEApr 20, 2026
51316-511-781 BOTTLE in 1 CARTON (51316-511-78) / 100 TABLET, FILM COATED in 1 BOTTLEApr 22, 2026
51316-511-981 BOTTLE in 1 CARTON (51316-511-98) / 75 TABLET, FILM COATED in 1 BOTTLEJun 24, 2026

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