NDC 21130-191 – Famotidine

Famotidine 20 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC21130-191

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
SAFEWAY
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA215822
Marketed since
June 30, 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
21130-191-20200 TABLET in 1 BOTTLE (21130-191-20)Jun 30, 2023

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