NDC 70756-051 – Famotidine

Famotidine 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70756-051

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Lifestar Pharma LLC
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 (2)

Package NDCDescriptionSince
70756-051-11100 TABLET in 1 BOTTLE (70756-051-11)Oct 19, 2023
70756-051-121000 TABLET in 1 BOTTLE (70756-051-12)Oct 19, 2023

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