Rubraca 200 mg Film-coated tablet

Licence status
Authorised: 24/05/2018
Active substances
Rucaparib camsylate
Dosage Form
Film-coated tablet
Licence number
EU/1/17/1250/001
Licence holder
pharmaand GmbH

Product documents

Licence information

ATC code
L01XX Other antineoplastic agents, L01XX55 Rucaparib
Legal supply status
Product subject to prescription which may not be renewed (A)
Place of sale
Supply through pharmacies only
Conditions of Licence
Medicinal product subject to restricted medical prescription (see Annex I: Summary of Product Characteristics, section 4.2).
Marketing availability
Unknown
Advertising conditions
Advertising to healthcare professionals only
Licence issued
24/05/2018