NDC 68071-3420 – Famotidine

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

Human Prescription Drug

Product NDC68071-3420

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215630
Marketed since
July 8, 2022
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (5)

Package NDCDescriptionSince
68071-3420-330 TABLET, FILM COATED in 1 BOTTLE (68071-3420-3)Jul 26, 2023
68071-3420-660 TABLET, FILM COATED in 1 BOTTLE (68071-3420-6)Jun 1, 2023
68071-3420-714 TABLET, FILM COATED in 1 BOTTLE (68071-3420-7)Jul 26, 2023
68071-3420-8120 TABLET, FILM COATED in 1 BOTTLE (68071-3420-8)Jul 26, 2023
68071-3420-990 TABLET, FILM COATED in 1 BOTTLE (68071-3420-9)Jul 26, 2023

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