NDC 55681-342 – Famotidine

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

Human Otc Drug

Product NDC55681-342

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
TWIN MED LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215822
Marketed since
January 28, 2022
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
55681-342-03300 TABLET, FILM COATED in 1 BOTTLE (55681-342-03)Sep 7, 2022

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