NDC 68788-8733 – Famotidine

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

Human Prescription Drug

Product NDC68788-8733

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215767
Marketed since
September 16, 2024
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
68788-8733-330 TABLET, FILM COATED in 1 BOTTLE (68788-8733-3)Sep 16, 2024
68788-8733-414 TABLET, FILM COATED in 1 BOTTLE (68788-8733-4)Sep 16, 2024
68788-8733-660 TABLET, FILM COATED in 1 BOTTLE (68788-8733-6)Sep 16, 2024
68788-8733-990 TABLET, FILM COATED in 1 BOTTLE (68788-8733-9)Sep 16, 2024

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