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 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: | 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: