NDC 71335-1950 – Famotidine

Famotidine 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-1950

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA075718
Marketed since
April 16, 2001
Listing expires
December 31, 2027
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (10)

Package NDCDescriptionSince
71335-1950-040 TABLET, FILM COATED in 1 BOTTLE (71335-1950-0)Mar 31, 2026
71335-1950-130 TABLET, FILM COATED in 1 BOTTLE (71335-1950-1)Mar 31, 2026
71335-1950-260 TABLET, FILM COATED in 1 BOTTLE (71335-1950-2)Mar 31, 2026
71335-1950-320 TABLET, FILM COATED in 1 BOTTLE (71335-1950-3)Mar 31, 2026
71335-1950-490 TABLET, FILM COATED in 1 BOTTLE (71335-1950-4)Mar 31, 2026
71335-1950-5100 TABLET, FILM COATED in 1 BOTTLE (71335-1950-5)Mar 31, 2026
71335-1950-610 TABLET, FILM COATED in 1 BOTTLE (71335-1950-6)Mar 31, 2026
71335-1950-7120 TABLET, FILM COATED in 1 BOTTLE (71335-1950-7)Mar 31, 2026
71335-1950-850 TABLET, FILM COATED in 1 BOTTLE (71335-1950-8)Mar 31, 2026
71335-1950-914 TABLET, FILM COATED in 1 BOTTLE (71335-1950-9)Mar 31, 2026

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