NDC 67877-842 – Famotidine

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

Human Prescription Drug

Product NDC67877-842

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215630
Marketed since
July 8, 2022
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (3)

Package NDCDescriptionSince
67877-842-01100 TABLET, FILM COATED in 1 BOTTLE (67877-842-01)Jul 8, 2022
67877-842-05500 TABLET, FILM COATED in 1 BOTTLE (67877-842-05)Feb 3, 2025
67877-842-101000 TABLET, FILM COATED in 1 BOTTLE (67877-842-10)Jul 8, 2022

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