NDC 69367-401 – Famotidine

Famotidine 40 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC69367-401

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Westminster Pharmaceuticals, LLC
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA217669
Marketed since
September 9, 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
69367-401-101000 TABLET, COATED in 1 BOTTLE, PLASTIC (69367-401-10)Sep 9, 2024

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