NDC 68788-4088 – Famotidine

Famotidine 20 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC68788-4088

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA217669
Marketed since
March 17, 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
68788-4088-330 TABLET, COATED in 1 BOTTLE, PLASTIC (68788-4088-3)Mar 17, 2026
68788-4088-414 TABLET, COATED in 1 BOTTLE, PLASTIC (68788-4088-4)Mar 17, 2026
68788-4088-660 TABLET, COATED in 1 BOTTLE, PLASTIC (68788-4088-6)Mar 17, 2026
68788-4088-990 TABLET, COATED in 1 BOTTLE, PLASTIC (68788-4088-9)Mar 17, 2026

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