FARYDAK (Novartis Pharmaceuticals Corporation)


Welcome to the PulseAid listing for the FARYDAK drug offered from Novartis Pharmaceuticals Corporation. This Histone Deacetylase Inhibitor [EPC],Histone Deacetylase Inhibitors [MoA],Cytochrome P450 2D6 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: panobinostat
SUBSTANCE NAME: PANOBINOSTAT LACTATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Histone Deacetylase Inhibitor [EPC],Histone Deacetylase Inhibitors [MoA],Cytochrome P450 2D6 Inhibitors [MoA]
ROUTE: ORAL
DOSAGE FORM: CAPSULE
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2015-02-23
END MARKETING DATE: 0000-00-00


FARYDAK HUMAN PRESCRIPTION DRUG Details:

Item DescriptionFARYDAK from Novartis Pharmaceuticals Corporation
LABELER NAME: Novartis Pharmaceuticals Corporation
DEA SCHEDULE:
ACTIVE STRENGTH: 10(mg/1)
START MARKETING DATE: 2015-02-23
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0078-0650_441444be-7168-4782-8219-c790b8f0bbde
PRODUCT NDC: 0078-0650
APPLICATION NUMBER: NDA205353

Other PANOBINOSTAT LACTATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Novartis Pharmaceuticals CorporationFARYDAK