Docetaxel (Teva Parenteral Medicines, Inc.)
Welcome to the PulseAid listing for the Docetaxel drug offered from Teva Parenteral Medicines, Inc.. 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: | Teva Parenteral Medicines, Inc. |
| NON-PROPRIETARY NAME: | Docetaxel |
| SUBSTANCE NAME: | DOCETAXEL ANHYDROUS |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Microtubule Inhibition [PE],Microtubule Inhibitor [EPC] |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION, CONCENTRATE |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2016-02-11 |
| END MARKETING DATE: | 0000-00-00 |
Docetaxel HUMAN PRESCRIPTION DRUG Details:
| Item Description | Docetaxel from Teva Parenteral Medicines, Inc. |
| LABELER NAME: | Teva Parenteral Medicines, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 20(mg/mL) |
| START MARKETING DATE: | 2016-02-11 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0703-5720_041cf665-2c3c-4c18-b7c8-d774e00d5aea |
| PRODUCT NDC: | 0703-5720 |
| APPLICATION NUMBER: | ANDA203877 |
Other DOCETAXEL ANHYDROUS Pharmaceutical Manufacturers / Labelers:
