NDC 68788-4144 – Famotidine

Famotidine 40 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC68788-4144

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
August 12, 2026
Listing expires
December 31, 2027
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (4)

Package NDCDescriptionSince
68788-4144-330 TABLET, FILM COATED in 1 BOTTLE (68788-4144-3)Aug 12, 2026
68788-4144-414 TABLET, FILM COATED in 1 BOTTLE (68788-4144-4)Aug 12, 2026
68788-4144-660 TABLET, FILM COATED in 1 BOTTLE (68788-4144-6)Aug 12, 2026
68788-4144-990 TABLET, FILM COATED in 1 BOTTLE (68788-4144-9)Aug 12, 2026

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