NDC 68788-8485 – Famotidine

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

Human Prescription Drug

Product NDC68788-8485

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215630
Marketed since
July 18, 2023
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
68788-8485-330 TABLET, FILM COATED in 1 BOTTLE (68788-8485-3)Jul 18, 2023
68788-8485-414 TABLET, FILM COATED in 1 BOTTLE (68788-8485-4)Jul 18, 2023
68788-8485-660 TABLET, FILM COATED in 1 BOTTLE (68788-8485-6)Jul 18, 2023
68788-8485-990 TABLET, FILM COATED in 1 BOTTLE (68788-8485-9)Jul 18, 2023

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