NDC 67877-668 – Febuxostat

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

Human Prescription Drug

Product NDC67877-668

Product details

Brand name
Febuxostat
Generic name
Febuxostat
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA212924
Marketed since
December 8, 2021
Listing expires
December 31, 2026
Pharmacologic class
Xanthine Oxidase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Febuxostat →

Package NDC codes (4)

Package NDCDescriptionSince
67877-668-101000 TABLET, FILM COATED in 1 BOTTLE (67877-668-10)Dec 8, 2021
67877-668-3030 TABLET, FILM COATED in 1 BOTTLE (67877-668-30)Dec 8, 2021
67877-668-3810 BLISTER PACK in 1 CARTON (67877-668-38) / 10 TABLET, FILM COATED in 1 BLISTER PACKDec 8, 2021
67877-668-9090 TABLET, FILM COATED in 1 BOTTLE (67877-668-90)Dec 8, 2021

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