ProHance (Bracco Diagnostics Inc)


Welcome to the PulseAid listing for the ProHance drug offered from Bracco Diagnostics Inc. This Magnetic Resonance Contrast Activity [MoA],Paramagnetic Contrast Agent [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: Bracco Diagnostics Inc
NON-PROPRIETARY NAME: gadoteridol
SUBSTANCE NAME: GADOTERIDOL
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Magnetic Resonance Contrast Activity [MoA],Paramagnetic Contrast Agent [EPC]
ROUTE: INTRAVENOUS
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2003-10-09
END MARKETING DATE: 0000-00-00


ProHance HUMAN PRESCRIPTION DRUG Details:

Item DescriptionProHance from Bracco Diagnostics Inc
LABELER NAME: Bracco Diagnostics Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 279.3(mg/mL)
START MARKETING DATE: 2003-10-09
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0270-1111_56b87355-3ad8-7109-744d-2e15a8e8e5a1
PRODUCT NDC: 0270-1111
APPLICATION NUMBER: NDA021489

Other GADOTERIDOL Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Bracco Diagnostics IncProHance
BRACCO DIAGNOSTICS INCProHance