NDC 67296-2133 – Famotidine

Famotidine 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC67296-2133

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Redpharm Drug
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075302
Marketed since
October 19, 2023
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
67296-2133-330 TABLET in 1 BOTTLE (67296-2133-3)Oct 19, 2023

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