NDC 68071-3786 – Famotidine

Famotidine 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC68071-3786

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215767
Marketed since
November 4, 2021
Listing expires
December 31, 2027
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (2)

Package NDCDescriptionSince
68071-3786-330 TABLET, FILM COATED in 1 BOTTLE (68071-3786-3)Jan 29, 2025
68071-3786-660 TABLET, FILM COATED in 1 BOTTLE (68071-3786-6)Sep 16, 2026

Other Famotidine products