NDC 71335-9724 – Famotidine

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

Human Prescription Drug

Product NDC71335-9724

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215630
Marketed since
July 8, 2022
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
71335-9724-130 TABLET, FILM COATED in 1 BOTTLE (71335-9724-1)May 30, 2023
71335-9724-260 TABLET, FILM COATED in 1 BOTTLE (71335-9724-2)May 30, 2023
71335-9724-3100 TABLET, FILM COATED in 1 BOTTLE (71335-9724-3)May 30, 2023
71335-9724-490 TABLET, FILM COATED in 1 BOTTLE (71335-9724-4)May 30, 2023
71335-9724-515 TABLET, FILM COATED in 1 BOTTLE (71335-9724-5)May 30, 2023
71335-9724-6120 TABLET, FILM COATED in 1 BOTTLE (71335-9724-6)May 30, 2023
71335-9724-720 TABLET, FILM COATED in 1 BOTTLE (71335-9724-7)May 30, 2023

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