NDC 71205-276 – Famotidine

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

Human Prescription Drug

Product NDC71205-276

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, 2027
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (7)

Package NDCDescriptionSince
71205-276-066 TABLET, FILM COATED in 1 BOTTLE (71205-276-06)Jul 8, 2021
71205-276-1010 TABLET, FILM COATED in 1 BOTTLE (71205-276-10)May 1, 2019
71205-276-3030 TABLET, FILM COATED in 1 BOTTLE (71205-276-30)May 1, 2019
71205-276-6060 TABLET, FILM COATED in 1 BOTTLE (71205-276-60)May 1, 2019
71205-276-67270 TABLET, FILM COATED in 1 BOTTLE (71205-276-67)Sep 23, 2024
71205-276-78180 TABLET, FILM COATED in 1 BOTTLE (71205-276-78)Jul 10, 2025
71205-276-9090 TABLET, FILM COATED in 1 BOTTLE (71205-276-90)Mar 13, 2026

Other Famotidine products