NDC 83324-008 – Famotidine

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

Human Otc Drug

Product NDC83324-008

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
CHAIN DRUG MARKETING ASSOCIATION, INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215766
Marketed since
March 6, 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 (1)

Package NDCDescriptionSince
83324-008-501 CONTAINER in 1 CARTON (83324-008-50) / 50 TABLET, FILM COATED in 1 CONTAINERMar 6, 2024

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