NDC 16714-059 – Febuxostat

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

Human Prescription Drug 2 recalls

Product NDC16714-059

Product details

Brand name
Febuxostat
Generic name
Febuxostat
Labeler
NorthStar RxLLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA205467
Marketed since
January 26, 2021
Listing expires
December 31, 2026
Pharmacologic class
Xanthine Oxidase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Febuxostat →

Package NDC codes (1)

Package NDCDescriptionSince
16714-059-0130 TABLET, FILM COATED in 1 BOTTLE (16714-059-01)Jan 26, 2021

Recalls mentioning this NDC

Other Febuxostat products