NDC 46708-191 – Febuxostat

Febuxostat 80 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC46708-191

Product details

Brand name
Febuxostat
Generic name
Febuxostat
Labeler
Alembic Pharmaceuticals Limited
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA205421
Marketed since
July 1, 2019
Listing expires
December 31, 2026
Pharmacologic class
Xanthine Oxidase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Febuxostat →

Package NDC codes (5)

Package NDCDescriptionSince
46708-191-0660 TABLET, COATED in 1 CARTON (46708-191-06)Jul 1, 2019
46708-191-10100 TABLET, COATED in 1 CARTON (46708-191-10)Jul 1, 2019
46708-191-3030 TABLET, COATED in 1 BOTTLE (46708-191-30)Jul 1, 2019
46708-191-31100 TABLET, COATED in 1 BOTTLE (46708-191-31)Jul 1, 2019
46708-191-911000 TABLET, COATED in 1 BOTTLE (46708-191-91)Jul 1, 2019

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