Rubraca (Clovis Oncology, Inc.)


Welcome to the PulseAid listing for the Rubraca drug offered from Clovis Oncology, Inc.. This Poly(ADP-Ribose) Polymerase Inhibitor [EPC],Poly(ADP-Ribose) Polymerase Inhibitors [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: Clovis Oncology, Inc.
NON-PROPRIETARY NAME: rucaparib
SUBSTANCE NAME: RUCAPARIB CAMSYLATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Poly(ADP-Ribose) Polymerase Inhibitor [EPC],Poly(ADP-Ribose) Polymerase Inhibitors [MoA]
ROUTE: ORAL
DOSAGE FORM: TABLET, FILM COATED
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2016-12-19
END MARKETING DATE: 0000-00-00


Rubraca HUMAN PRESCRIPTION DRUG Details:

Item DescriptionRubraca from Clovis Oncology, Inc.
LABELER NAME: Clovis Oncology, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 200(mg/1)
START MARKETING DATE: 2016-12-19
END MARKETING DATE: 0000-00-00
PRODUCT ID: 69660-201_acb1cfd2-6ab1-4051-921c-225718e1f10f
PRODUCT NDC: 69660-201
APPLICATION NUMBER: NDA209115

Other RUCAPARIB CAMSYLATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Clovis Oncology, Inc.Rubraca