NDC 85534-0092 – Famotidine

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

Human Prescription Drug

Product NDC85534-0092

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
HAWAII REPACK, INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215630
Marketed since
August 23, 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
85534-0092-030 TABLET, FILM COATED in 1 BOTTLE (85534-0092-0)Jul 13, 2026
85534-0092-160 TABLET, FILM COATED in 1 BOTTLE (85534-0092-1)Jul 13, 2026
85534-0092-290 TABLET, FILM COATED in 1 BOTTLE (85534-0092-2)Jul 13, 2026
85534-0092-3120 TABLET, FILM COATED in 1 BOTTLE (85534-0092-3)Jul 13, 2026

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