NDC 68071-4197 – Famotidine

Famotidine 40 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-4197

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 (3)

Package NDCDescriptionSince
68071-4197-330 TABLET in 1 BOTTLE (68071-4197-3)Dec 20, 2017
68071-4197-660 TABLET in 1 BOTTLE (68071-4197-6)Dec 20, 2017
68071-4197-990 TABLET in 1 BOTTLE (68071-4197-9)Dec 20, 2017

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