NDC 49035-505 – Famotidine

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

Human Otc Drug

Product NDC49035-505

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Wal-Mart Stores, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA206531
Marketed since
April 26, 2016
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (7)

Package NDCDescriptionSince
49035-505-141 BOTTLE in 1 CARTON (49035-505-14) / 50 TABLET, FILM COATED in 1 BOTTLEAug 6, 2020
49035-505-211 BOTTLE in 1 CARTON (49035-505-21) / 100 TABLET, FILM COATED in 1 BOTTLEAug 6, 2020
49035-505-341 BOTTLE in 1 CARTON (49035-505-34) / 200 TABLET, FILM COATED in 1 BOTTLEAug 6, 2020
49035-505-351 BOTTLE in 1 CARTON (49035-505-35) / 25 TABLET, FILM COATED in 1 BOTTLEApr 26, 2016
49035-505-391 BOTTLE in 1 CARTON (49035-505-39) / 365 TABLET, FILM COATED in 1 BOTTLEJan 21, 2021
49035-505-802 BOTTLE in 1 CARTON (49035-505-80) / 100 TABLET, FILM COATED in 1 BOTTLEAug 6, 2020
49035-505-952 BOTTLE in 1 CARTON (49035-505-95) / 50 TABLET, FILM COATED in 1 BOTTLEAug 6, 2020

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