ZELBORAF (Genentech, Inc.)


Welcome to the PulseAid listing for the ZELBORAF drug offered from Genentech, Inc.. This Kinase Inhibitor [EPC],Protein Kinase Inhibitors [MoA],Cytochrome P450 1A2 Inhibitors [MoA],P-Glycoprotein 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: Genentech, Inc.
NON-PROPRIETARY NAME: Vemurafenib
SUBSTANCE NAME: VEMURAFENIB
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Kinase Inhibitor [EPC],Protein Kinase Inhibitors [MoA],Cytochrome P450 1A2 Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA]
ROUTE: ORAL
DOSAGE FORM: TABLET, FILM COATED
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2011-08-17
END MARKETING DATE: 0000-00-00


ZELBORAF HUMAN PRESCRIPTION DRUG Details:

Item DescriptionZELBORAF from Genentech, Inc.
LABELER NAME: Genentech, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 240(mg/1)
START MARKETING DATE: 2011-08-17
END MARKETING DATE: 0000-00-00
PRODUCT ID: 50242-090_12027f5f-f87f-4551-9ca0-1978bfbd1494
PRODUCT NDC: 50242-090
APPLICATION NUMBER: NDA202429

Other VEMURAFENIB Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Genentech, Inc.ZELBORAF