NDC 71205-781 – Famotidine

Famotidine 40 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71205-781

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA075511
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 (3)

Package NDCDescriptionSince
71205-781-3030 TABLET, FILM COATED in 1 BOTTLE (71205-781-30)Mar 27, 2023
71205-781-6060 TABLET, FILM COATED in 1 BOTTLE (71205-781-60)Mar 27, 2023
71205-781-9090 TABLET, FILM COATED in 1 BOTTLE (71205-781-90)Mar 27, 2023

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