NDC 55154-4313 – Famotidine

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

Human Prescription Drug

Product NDC55154-4313

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Cardinal Health 107, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA075718
Marketed since
April 16, 2001
Listing expires
December 31, 2027
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (1)

Package NDCDescriptionSince
55154-4313-010 BLISTER PACK in 1 BAG (55154-4313-0) / 1 TABLET, FILM COATED in 1 BLISTER PACKMar 15, 2023

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