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 Description | ProHance from BRACCO DIAGNOSTICS INC |
LABELER NAME: | BRACCO DIAGNOSTICS INC |
DEA SCHEDULE: |
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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: