ULORIC - 64764-677-19 - (febuxostat)

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Drug Information of ULORIC

Product NDC: 64764-677
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: 64764-677
Labeler Name: Takeda Pharmaceuticals America, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021856
Marketing Category: NDA
Start Marketing Date: 20090213

Package Information of ULORIC

Package NDC: 64764-677-19
Package Description: 1000 TABLET in 1 BOTTLE (64764-677-19)

NDC Information of ULORIC

NDC Code 64764-677-19
Proprietary Name ULORIC
Package Description 1000 TABLET in 1 BOTTLE (64764-677-19)
Product NDC 64764-677
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 Takeda Pharmaceuticals America, Inc.
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