NDC 68071-3761 – Febuxostat

Febuxostat 80 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC68071-3761

Product details

Brand name
Febuxostat
Generic name
Febuxostat
Labeler
NuCare Pharmaceuticals, Inc.
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
68071-3761-990 TABLET, FILM COATED in 1 BOTTLE (68071-3761-9)Jan 10, 2025

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