Mannitol (Cardinal Health)


Welcome to the PulseAid listing for the Mannitol drug offered from Cardinal Health. 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: Cardinal Health
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: 2010-02-01
END MARKETING DATE: 0000-00-00


Mannitol HUMAN PRESCRIPTION DRUG Details:

Item DescriptionMannitol from Cardinal Health
LABELER NAME: Cardinal Health
DEA SCHEDULE:
ACTIVE STRENGTH: 12.5(g/50mL)
START MARKETING DATE: 2010-02-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 55154-3192_3d28e213-4643-4fd7-ad87-5911f89368ef
PRODUCT NDC: 55154-3192
APPLICATION NUMBER: NDA016269

Other MANNITOL Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
American Regent, Inc.Mannitol
B. Braun Medical Inc.Mannitol
Baxter Healthcare CorporationOsmitrol
Cardinal HealthMannitol
Coson Co., Ltd.GD11 Rx SCM C5
Fresenius Kabi USA, LLCMannitol
General Injectables & Vaccines, IncMannitol
Hospira, Inc.Mannitol