NDC 72162-1737 – Famotidine

Famotidine 40 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72162-1737

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075805
Marketed since
April 16, 2001
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (2)

Package NDCDescriptionSince
72162-1737-01000 TABLET in 1 BOTTLE (72162-1737-0)Sep 17, 2024
72162-1737-1100 TABLET in 1 BOTTLE (72162-1737-1)Sep 17, 2024

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