Mannitol (B. Braun Medical Inc.)


Welcome to the PulseAid listing for the Mannitol drug offered from B. Braun Medical 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: B. Braun Medical 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: 1993-07-26
END MARKETING DATE: 0000-00-00


Mannitol HUMAN PRESCRIPTION DRUG Details:

Item DescriptionMannitol from B. Braun Medical Inc.
LABELER NAME: B. Braun Medical Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 20(g/100mL)
START MARKETING DATE: 1993-07-26
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0264-7578_4e259082-1a2c-43c9-a4ab-85a27b7a468e
PRODUCT NDC: 0264-7578
APPLICATION NUMBER: NDA020006

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