VOTRIENT - 0173-0804-61 - (pazopanib hydrochloride)

Alphabetical Index


Drug Information of VOTRIENT

Product NDC: 0173-0804
Proprietary Name: VOTRIENT
Non Proprietary Name: pazopanib hydrochloride
Active Ingredient(s): 200    mg/1 & nbsp;   pazopanib hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of VOTRIENT

Product NDC: 0173-0804
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022465
Marketing Category: NDA
Start Marketing Date: 20091019

Package Information of VOTRIENT

Package NDC: 0173-0804-61
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (0173-0804-61)

NDC Information of VOTRIENT

NDC Code 0173-0804-61
Proprietary Name VOTRIENT
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (0173-0804-61)
Product NDC 0173-0804
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name pazopanib hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20091019
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name PAZOPANIB HYDROCHLORIDE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Kinase Inhibitor [EPC]

Complete Information of VOTRIENT


General Information