NDC 68071-2306 – Famotidine

Famotidine 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-2306

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075805
Marketed since
April 16, 2001
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
68071-2306-330 TABLET in 1 BOTTLE (68071-2306-3)Nov 30, 2020
68071-2306-8180 TABLET in 1 BOTTLE (68071-2306-8)Nov 30, 2020

Other Famotidine products