Sorbitol-Mannitol (Hospira, Inc.)
Welcome to the PulseAid listing for the Sorbitol-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: | SORBITOL and MANNITOL |
SUBSTANCE NAME: | SORBITOL; MANNITOL |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Increased Diuresis [PE],Osmotic Activity [MoA],Osmotic Diuretic [EPC] |
ROUTE: | URETHRAL |
DOSAGE FORM: | IRRIGANT |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2005-05-24 |
END MARKETING DATE: | 0000-00-00 |
Sorbitol-Mannitol HUMAN PRESCRIPTION DRUG Details:
Item Description | Sorbitol-Mannitol from Hospira, Inc. |
LABELER NAME: | Hospira, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 2.7; .54(g/100mL; g/100mL) |
START MARKETING DATE: | 2005-05-24 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0409-7981_21ea390d-ede6-449c-a4e6-e2756f6ca2ee |
PRODUCT NDC: | 0409-7981 |
APPLICATION NUMBER: | NDA018316 |
Other SORBITOL; MANNITOL Pharmaceutical Manufacturers / Labelers: