RYDAPT (Novartis Pharmaceuticals Corporation)


Welcome to the PulseAid listing for the RYDAPT drug offered from Novartis Pharmaceuticals Corporation. This Kinase Inhibitor [EPC],Receptor Tyrosine Kinase 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: RYDAPT
SUBSTANCE NAME: MIDOSTAURIN
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Kinase Inhibitor [EPC],Receptor Tyrosine Kinase Inhibitors [MoA]
ROUTE: ORAL
DOSAGE FORM: CAPSULE, LIQUID FILLED
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2017-04-28
END MARKETING DATE: 0000-00-00


RYDAPT HUMAN PRESCRIPTION DRUG Details:

Item DescriptionRYDAPT from Novartis Pharmaceuticals Corporation
LABELER NAME: Novartis Pharmaceuticals Corporation
DEA SCHEDULE:
ACTIVE STRENGTH: 25(mg/1)
START MARKETING DATE: 2017-04-28
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0078-0698_11fa3fc9-6776-49a6-b1c1-653f627c3e58
PRODUCT NDC: 0078-0698
APPLICATION NUMBER: NDA207997

Other MIDOSTAURIN Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Novartis Pharmaceuticals CorporationRYDAPT