KISQALI (Novartis Pharmaceuticals Corporation)


Welcome to the PulseAid listing for the KISQALI drug offered from Novartis Pharmaceuticals Corporation. This Kinase Inhibitor [EPC],Kinase Inhibitors [MoA],Cytochrome P450 3A 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: Novartis Pharmaceuticals Corporation
NON-PROPRIETARY NAME: ribociclib
SUBSTANCE NAME: RIBOCICLIB
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Kinase Inhibitor [EPC],Kinase Inhibitors [MoA],Cytochrome P450 3A Inhibitors [MoA]
ROUTE: ORAL
DOSAGE FORM: TABLET, FILM COATED
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2017-03-13
END MARKETING DATE: 0000-00-00


KISQALI HUMAN PRESCRIPTION DRUG Details:

Item DescriptionKISQALI from Novartis Pharmaceuticals Corporation
LABELER NAME: Novartis Pharmaceuticals Corporation
DEA SCHEDULE:
ACTIVE STRENGTH: 200(mg/1)
START MARKETING DATE: 2017-03-13
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0078-0860_11364b70-4e7c-49de-8e2c-17c35a22e36f
PRODUCT NDC: 0078-0860
APPLICATION NUMBER: NDA209092

Other RIBOCICLIB Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Novartis Pharmaceuticals CorporationKISQALI