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Rubraca



Clovis Oncology Ireland LimitedEU/1/17/1250/003

Main Information

Trade NameRubraca
Active SubstancesRucaparib camsylate
Dosage FormFilm-coated tablet
Licence HolderClovis Oncology Ireland Limited
Licence NumberEU/1/17/1250/003

Group Information

ATC CodeL01XX Other antineoplastic agents
L01XX55 Rucaparib

Status

License statusAuthorised
Licence Issued24/05/2018
Legal statusProduct subject to prescription which may not be renewed (A)
Supply StatusSupply through pharmacies only
Advertising StatusAdvertising to healthcare professionals only
Conditions of LicenceMedicinal product subject to restricted medical prescription (see Annex I: Summary of Product Characteristics, section 4.2).
Marketing StatusUnknown

Documents

Summary of Product CharacteristicsSearch EMA website
Package LeafletSearch EMA website
Public Assessment ReportSearch EMA website
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