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 the 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 DescriptionSorbitol-Mannitol from Hospira, Inc.
LABELER NAME: Hospira, Inc.
DEA SCHEDULE:
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:

Manufacturer / LabelerProprietary Name
Hospira, Inc.Sorbitol-Mannitol