Odomzo (Novartis Pharmaceuticals Corporation)


Welcome to the PulseAid listing for the Odomzo drug offered from Novartis Pharmaceuticals Corporation. This Hedgehog Pathway Inhibitor [EPC],Smoothened Receptor Antagonists [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: sonidegib
SUBSTANCE NAME: SONIDEGIB PHOSPHATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Hedgehog Pathway Inhibitor [EPC],Smoothened Receptor Antagonists [MoA]
ROUTE: ORAL
DOSAGE FORM: CAPSULE
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2015-07-24
END MARKETING DATE: 2017-12-31


Odomzo HUMAN PRESCRIPTION DRUG Details:

Item DescriptionOdomzo from Novartis Pharmaceuticals Corporation
LABELER NAME: Novartis Pharmaceuticals Corporation
DEA SCHEDULE:
ACTIVE STRENGTH: 200(mg/1)
START MARKETING DATE: 2015-07-24
END MARKETING DATE: 2017-12-31
PRODUCT ID: 0078-0645_33db8080-93db-4c75-91ad-d5b96b4c7b41
PRODUCT NDC: 0078-0645
APPLICATION NUMBER: NDA205266

Other SONIDEGIB PHOSPHATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Novartis Pharmaceuticals CorporationOdomzo
Sun Pharma Global FZEOdomzo