NDC 47335-721 – Febuxostat

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

Human Prescription Drug 2 recalls

Product NDC47335-721

Product details

Brand name
Febuxostat
Generic name
Febuxostat
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA205467
Marketed since
July 5, 2019
Listing expires
December 31, 2026
Pharmacologic class
Xanthine Oxidase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Febuxostat →

Package NDC codes (3)

Package NDCDescriptionSince
47335-721-13500 TABLET, FILM COATED in 1 BOTTLE (47335-721-13)Jul 5, 2019
47335-721-8190 TABLET, FILM COATED in 1 BOTTLE (47335-721-81)Jul 5, 2019
47335-721-8330 TABLET, FILM COATED in 1 BOTTLE (47335-721-83)Jul 5, 2019

Recalls mentioning this NDC

Other Febuxostat products