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: 1992-11-16
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: 1992-11-16
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0270-1111_af96951b-3335-4f89-b474-0423bc93b813
PRODUCT NDC: 0270-1111
APPLICATION NUMBER: NDA020131

Other GADOTERIDOL Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Bracco Diagnostics IncProHance
BRACCO DIAGNOSTICS INCProHance