Deferoxamine Mesylate (Hospira, Inc.)
Welcome to the PulseAid listing for the Deferoxamine Mesylate drug offered from Hospira, Inc.. This Iron Chelating Activity [MoA],Iron Chelator [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: | Hospira, Inc. |
| NON-PROPRIETARY NAME: | Deferoxamine Mesylate |
| SUBSTANCE NAME: | DEFEROXAMINE MESYLATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Iron Chelating Activity [MoA],Iron Chelator [EPC] |
| ROUTE: | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| DOSAGE FORM: | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2005-04-30 |
| END MARKETING DATE: | 0000-00-00 |
Deferoxamine Mesylate HUMAN PRESCRIPTION DRUG Details:
| Item Description | Deferoxamine Mesylate from Hospira, Inc. |
| LABELER NAME: | Hospira, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 500(mg/1) |
| START MARKETING DATE: | 2005-04-30 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0409-2336_6780d57f-ba00-4928-9203-2877b414467f |
| PRODUCT NDC: | 0409-2336 |
| APPLICATION NUMBER: | ANDA076019 |
Other DEFEROXAMINE MESYLATE Pharmaceutical Manufacturers / Labelers:
