Xofigo (Bayer HealthCare Pharmaceuticals Inc.)


Welcome to the PulseAid listing for the Xofigo drug offered from Bayer HealthCare Pharmaceuticals Inc.. This Radioactive alpha-Particle Emitting Therapeutic Agent [EPC],alpha-Particle Emitting Activity [MoA] 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: Bayer HealthCare Pharmaceuticals Inc.
NON-PROPRIETARY NAME: Radium Ra 223 dichloride
SUBSTANCE NAME: RADIUM RA-223 DICHLORIDE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Radioactive alpha-Particle Emitting Therapeutic Agent [EPC],alpha-Particle Emitting Activity [MoA]
ROUTE: INTRAVENOUS
DOSAGE FORM: INJECTION
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2013-05-20
END MARKETING DATE: 0000-00-00


Xofigo HUMAN PRESCRIPTION DRUG Details:

Item DescriptionXofigo from Bayer HealthCare Pharmaceuticals Inc.
LABELER NAME: Bayer HealthCare Pharmaceuticals Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 30(uCi/mL)
START MARKETING DATE: 2013-05-20
END MARKETING DATE: 0000-00-00
PRODUCT ID: 50419-208_f45869fa-8747-4375-86cd-bfd46620d088
PRODUCT NDC: 50419-208
APPLICATION NUMBER: NDA203971

Other RADIUM RA-223 DICHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Bayer HealthCare Pharmaceuticals Inc.Xofigo