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 Description | Odomzo from Novartis Pharmaceuticals Corporation |
LABELER NAME: | Novartis Pharmaceuticals Corporation |
DEA SCHEDULE: |
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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: