NDC 68788-4021 – Famotidine

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

Human Prescription Drug

Product NDC68788-4021

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA217400
Marketed since
September 5, 2025
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (4)

Package NDCDescriptionSince
68788-4021-330 TABLET, FILM COATED in 1 BOTTLE (68788-4021-3)Sep 5, 2025
68788-4021-414 TABLET, FILM COATED in 1 BOTTLE (68788-4021-4)Sep 5, 2025
68788-4021-660 TABLET, FILM COATED in 1 BOTTLE (68788-4021-6)Sep 5, 2025
68788-4021-990 TABLET, FILM COATED in 1 BOTTLE (68788-4021-9)Sep 5, 2025

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