NDC 37835-165 – Famotidine

Famotidine 20 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC37835-165

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Bi-Mart
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA215822
Marketed since
June 1, 2025
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
37835-165-5050 TABLET in 1 BOTTLE (37835-165-50)Jun 1, 2025

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