VOTRIENT (GlaxoSmithKline LLC)


Welcome to the PulseAid listing for the VOTRIENT drug offered from GlaxoSmithKline LLC. This Kinase Inhibitor [EPC],Protein Kinase Inhibitors [MoA],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 2D6 Inhibitors [MoA],Cytochrome P450 2C8 Inhibitors [MoA] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: GlaxoSmithKline LLC
NON-PROPRIETARY NAME: pazopanib hydrochloride
SUBSTANCE NAME: PAZOPANIB HYDROCHLORIDE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Kinase Inhibitor [EPC],Protein Kinase Inhibitors [MoA],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 2D6 Inhibitors [MoA],Cytochrome P450 2C8 Inhibitors [MoA]
ROUTE: ORAL
DOSAGE FORM: TABLET, FILM COATED
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2009-10-19
END MARKETING DATE: 2017-11-30


VOTRIENT HUMAN PRESCRIPTION DRUG Details:

Item DescriptionVOTRIENT from GlaxoSmithKline LLC
LABELER NAME: GlaxoSmithKline LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 200(mg/1)
START MARKETING DATE: 2009-10-19
END MARKETING DATE: 2017-11-30
PRODUCT ID: 0173-0804_7cc70c3d-7852-4de5-a116-194017e95017
PRODUCT NDC: 0173-0804
APPLICATION NUMBER: NDA022465

Other PAZOPANIB HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
GlaxoSmithKline LLCVOTRIENT
Novartis Pharmaceuticals CorporationVOTRIENT