ULORIC - 21695-516-30 - (febuxostat)

Alphabetical Index


Drug Information of ULORIC

Product NDC: 21695-516
Proprietary Name: ULORIC
Non Proprietary Name: febuxostat
Active Ingredient(s): 80    mg/1 & nbsp;   febuxostat
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of ULORIC

Product NDC: 21695-516
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021856
Marketing Category: NDA
Start Marketing Date: 20090213

Package Information of ULORIC

Package NDC: 21695-516-30
Package Description: 30 TABLET in 1 BOTTLE (21695-516-30)

NDC Information of ULORIC

NDC Code 21695-516-30
Proprietary Name ULORIC
Package Description 30 TABLET in 1 BOTTLE (21695-516-30)
Product NDC 21695-516
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name febuxostat
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090213
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp
Substance Name FEBUXOSTAT
Strength Number 80
Strength Unit mg/1
Pharmaceutical Classes Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]

Complete Information of ULORIC


General Information