NDC 71205-535 – Famotidine

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

Human Prescription Drug

Product NDC71205-535

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA206530
Marketed since
December 22, 2015
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (5)

Package NDCDescriptionSince
71205-535-066 TABLET, FILM COATED in 1 BOTTLE (71205-535-06)Feb 24, 2021
71205-535-1010 TABLET, FILM COATED in 1 BOTTLE (71205-535-10)Feb 24, 2021
71205-535-3030 TABLET, FILM COATED in 1 BOTTLE (71205-535-30)Feb 16, 2021
71205-535-6060 TABLET, FILM COATED in 1 BOTTLE (71205-535-60)Feb 16, 2021
71205-535-78180 TABLET, FILM COATED in 1 BOTTLE (71205-535-78)Sep 6, 2024

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