Floxuridine (Fresenius Kabi USA, LLC)
Welcome to the PulseAid listing for the Floxuridine drug offered from Fresenius Kabi USA, LLC. This Antimetabolite [EPC],Deoxyuridine [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: | Fresenius Kabi USA, LLC |
| NON-PROPRIETARY NAME: | FLOXURIDINE |
| SUBSTANCE NAME: | FLOXURIDINE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Antimetabolite [EPC],Deoxyuridine [Chemical/Ingredient] |
| ROUTE: | INTRA-ARTERIAL |
| DOSAGE FORM: | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2001-03-15 |
| END MARKETING DATE: | 0000-00-00 |
Floxuridine HUMAN PRESCRIPTION DRUG Details:
| Item Description | Floxuridine from Fresenius Kabi USA, LLC |
| LABELER NAME: | Fresenius Kabi USA, LLC |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 500(mg/5mL) |
| START MARKETING DATE: | 2001-03-15 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 63323-145_c27f9bb1-7621-4989-8dba-c8b9fa5503a8 |
| PRODUCT NDC: | 63323-145 |
| APPLICATION NUMBER: | ANDA075837 |
Other FLOXURIDINE Pharmaceutical Manufacturers / Labelers:
