Mannitol (Hospira, Inc.)
Welcome to the PulseAid listing for the Mannitol drug offered from Hospira, Inc.. This Increased Diuresis [PE],Osmotic Activity [MoA],Osmotic Diuretic [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: | MANNITOL |
| SUBSTANCE NAME: | MANNITOL |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Increased Diuresis [PE],Osmotic Activity [MoA],Osmotic Diuretic [EPC] |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 2004-11-30 |
| END MARKETING DATE: | 0000-00-00 |
Mannitol HUMAN PRESCRIPTION DRUG Details:
| Item Description | Mannitol from Hospira, Inc. |
| LABELER NAME: | Hospira, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 12.5(g/50mL) |
| START MARKETING DATE: | 2004-11-30 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0409-4031_48bfb4b7-7f48-479e-8f0f-09e746e34fa6 |
| PRODUCT NDC: | 0409-4031 |
| APPLICATION NUMBER: | NDA016269 |
Other MANNITOL Pharmaceutical Manufacturers / Labelers:
