Docetaxel (Winthrop U.S.)
Welcome to the PulseAid listing for the Docetaxel drug offered from Winthrop U.S.. This Microtubule Inhibition [PE],Microtubule Inhibitor [EPC] 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: | Winthrop U.S. |
| NON-PROPRIETARY NAME: | Docetaxel |
| SUBSTANCE NAME: | DOCETAXEL |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Microtubule Inhibition [PE],Microtubule Inhibitor [EPC] |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION, CONCENTRATE |
| MARKETING CATEGORY NAME: | NDA AUTHORIZED GENERIC |
| START MARKETING DATE: | 2010-10-21 |
| END MARKETING DATE: | 0000-00-00 |
Docetaxel HUMAN PRESCRIPTION DRUG Details:
| Item Description | Docetaxel from Winthrop U.S. |
| LABELER NAME: | Winthrop U.S. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 20(mg/mL) |
| START MARKETING DATE: | 2010-10-21 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0955-1020_ea887537-d6ab-45f3-8b8c-447e14f2722a |
| PRODUCT NDC: | 0955-1020 |
| APPLICATION NUMBER: | NDA020449 |
Other DOCETAXEL Pharmaceutical Manufacturers / Labelers:
