NDC 72205-146 – Famotidine

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

Human Prescription Drug

Product NDC72205-146

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Novadoz Pharmaceuticals LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA217400
Marketed since
August 6, 2024
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (4)

Package NDCDescriptionSince
72205-146-05500 TABLET, FILM COATED in 1 BOTTLE (72205-146-05)Sep 18, 2024
72205-146-3030 TABLET, FILM COATED in 1 BOTTLE (72205-146-30)Sep 18, 2024
72205-146-91100 TABLET, FILM COATED in 1 BOTTLE (72205-146-91)Sep 18, 2024
72205-146-991000 TABLET, FILM COATED in 1 BOTTLE (72205-146-99)Sep 18, 2024

Other Famotidine products