NDC 71335-1520 – Famotidine

Famotidine 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1520

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 (9)

Package NDCDescriptionSince
71335-1520-130 TABLET in 1 BOTTLE (71335-1520-1)Feb 20, 2020
71335-1520-260 TABLET in 1 BOTTLE (71335-1520-2)Mar 30, 2021
71335-1520-320 TABLET in 1 BOTTLE (71335-1520-3)Jul 14, 2022
71335-1520-490 TABLET in 1 BOTTLE (71335-1520-4)Feb 15, 2022
71335-1520-5100 TABLET in 1 BOTTLE (71335-1520-5)Sep 6, 2024
71335-1520-610 TABLET in 1 BOTTLE (71335-1520-6)Jun 29, 2021
71335-1520-7120 TABLET in 1 BOTTLE (71335-1520-7)Oct 7, 2021
71335-1520-850 TABLET in 1 BOTTLE (71335-1520-8)Sep 6, 2024
71335-1520-914 TABLET in 1 BOTTLE (71335-1520-9)Sep 6, 2024

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