NDC 69842-087 – Famotidine

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

Human Otc Drug

Product NDC69842-087

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
CVS Pharmacy, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA206531
Marketed since
February 3, 2020
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (5)

Package NDCDescriptionSince
69842-087-141 BOTTLE in 1 CARTON (69842-087-14) / 50 TABLET, FILM COATED in 1 BOTTLEFeb 3, 2020
69842-087-211 BOTTLE in 1 CARTON (69842-087-21) / 100 TABLET, FILM COATED in 1 BOTTLEFeb 3, 2020
69842-087-531 BOTTLE in 1 CARTON (69842-087-53) / 25 TABLET, FILM COATED in 1 BOTTLEFeb 3, 2020
69842-087-791 BLISTER PACK in 1 CARTON (69842-087-79) / 8 TABLET, FILM COATED in 1 BLISTER PACKDec 1, 2022
69842-087-802 BOTTLE in 1 CARTON (69842-087-80) / 100 TABLET, FILM COATED in 1 BOTTLEJan 25, 2021

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