NDC 63629-2782 – Famotidine

Famotidine 40 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC63629-2782

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 (7)

Package NDCDescriptionSince
63629-2782-130 TABLET in 1 BOTTLE (63629-2782-1)Mar 14, 2005
63629-2782-260 TABLET in 1 BOTTLE (63629-2782-2)Jun 26, 2007
63629-2782-3100 TABLET in 1 BOTTLE (63629-2782-3)Jul 16, 2007
63629-2782-490 TABLET in 1 BOTTLE (63629-2782-4)Dec 14, 2010
63629-2782-515 TABLET in 1 BOTTLE (63629-2782-5)Feb 4, 2013
63629-2782-6120 TABLET in 1 BOTTLE (63629-2782-6)May 4, 2015
63629-2782-720 TABLET in 1 BOTTLE (63629-2782-7)Sep 5, 2024

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