OXALIPLATIN (Winthrop U.S.)
Welcome to the PulseAid listing for the OXALIPLATIN drug offered from Winthrop U.S.. This Platinum-based Drug [EPC],Platinum-containing Compounds [Chemical/Ingredient] 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: | oxaliplatin |
| SUBSTANCE NAME: | OXALIPLATIN |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Platinum-based Drug [EPC],Platinum-containing Compounds [Chemical/Ingredient] |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION, CONCENTRATE |
| MARKETING CATEGORY NAME: | NDA AUTHORIZED GENERIC |
| START MARKETING DATE: | 2014-07-07 |
| END MARKETING DATE: | 0000-00-00 |
OXALIPLATIN HUMAN PRESCRIPTION DRUG Details:
| Item Description | OXALIPLATIN from Winthrop U.S. |
| LABELER NAME: | Winthrop U.S. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 5(mg/mL) |
| START MARKETING DATE: | 2014-07-07 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0955-1725_d8acf0f4-9a54-4b7d-86bb-848ea24e2b39 |
| PRODUCT NDC: | 0955-1725 |
| APPLICATION NUMBER: | NDA021759 |
Other OXALIPLATIN Pharmaceutical Manufacturers / Labelers:
