Mannitol (American Regent, Inc.)
Welcome to the PulseAid listing for the Mannitol drug offered from American Regent, 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: | American Regent, 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: | ANDA |
| START MARKETING DATE: | 1990-09-30 |
| END MARKETING DATE: | 0000-00-00 |
Mannitol HUMAN PRESCRIPTION DRUG Details:
| Item Description | Mannitol from American Regent, Inc. |
| LABELER NAME: | American Regent, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 250(mg/mL) |
| START MARKETING DATE: | 1990-09-30 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0517-4050_560eaf50-0d23-4df6-9068-eebba66634d4 |
| PRODUCT NDC: | 0517-4050 |
| APPLICATION NUMBER: | ANDA087409 |
Other MANNITOL Pharmaceutical Manufacturers / Labelers:
