Dexrazoxane (Breckenridge Pharmaceutical, Inc.)
Welcome to the PulseAid listing for the Dexrazoxane drug offered from Breckenridge Pharmaceutical, Inc.. This Cytoprotective Agent [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: | Breckenridge Pharmaceutical, Inc. |
| NON-PROPRIETARY NAME: | Dexrazoxane Hydrochloride |
| SUBSTANCE NAME: | DEXRAZOXANE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Cytoprotective Agent [EPC] |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2016-12-05 |
| END MARKETING DATE: | 0000-00-00 |
Dexrazoxane HUMAN PRESCRIPTION DRUG Details:
| Item Description | Dexrazoxane from Breckenridge Pharmaceutical, Inc. |
| LABELER NAME: | Breckenridge Pharmaceutical, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 500(mg/50mL) |
| START MARKETING DATE: | 2016-12-05 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 51991-942_46cc35ce-76d6-473e-a0bf-24d973c20791 |
| PRODUCT NDC: | 51991-942 |
| APPLICATION NUMBER: | ANDA207321 |
Other DEXRAZOXANE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
