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: IRRIGATION
DOSAGE FORM: IRRIGANT
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 1978-02-10
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: 5(g/100mL)
START MARKETING DATE: 1978-02-10
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0264-2303_a6df35d3-121c-42e9-ae15-5ca17bd286a2
PRODUCT NDC: 0264-2303
APPLICATION NUMBER: NDA016772

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