"0051-2677-30" National Drug Code (NDC)

NDC Code	0051-2677-30
Package Description	30 TABLET in 1 BOTTLE (0051-2677-30)
Product NDC	0051-2677
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Febuxostat
Non-Proprietary Name	Febuxostat
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20090213
End Marketing Date	20210531
Marketing Category Name	APPROVED DRUG PRODUCT MANUFACTURED UNDER CONTRACT
Application Number	NDA021856
Manufacturer	AbbVie Inc.
Substance Name	FEBUXOSTAT
Strength	80
Strength Unit	mg/1
Pharmacy Classes	Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]