NDC 72189-141 – Famotidine

Famotidine 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72189-141

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
direct rx
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078916
Marketed since
October 15, 2020
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (2)

Package NDCDescriptionSince
72189-141-6060 TABLET in 1 BOTTLE (72189-141-60)Oct 15, 2020
72189-141-9090 TABLET in 1 BOTTLE (72189-141-90)Oct 15, 2020

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