NDC 71821-012 – Famotidine

Famotidine 10 mg/1 · Tablet, Film Coated · Oral

Human Otc Drug

Product NDC71821-012

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
VKT Pharma Private Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215822
Marketed since
May 23, 2024
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (2)

Package NDCDescriptionSince
71821-012-08288461 TABLET, FILM COATED in 1 BAG (71821-012-08)Sep 7, 2022
71821-012-09288461 TABLET, FILM COATED in 1 BAG (71821-012-09)May 23, 2024

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