Prolevare RSSAuthorisedThis medicine is authorised for use in the European Unionoclacitinib maleateMedicineVeterinaryAuthorised
Page contentsOverviewProduct detailsAuthorisation detailsAssessment historyNews on ProlevareOverviewUp-to-date information on this veterinary medicinal product is available on the Veterinary Medicines Information website.Product detailsName of medicine Prolevare Active substance oclacitinib maleate International non-proprietary name (INN) or common name oclacitinib maleate Pharmacotherapeutic groupOther dermatological preparationsDermatologicalsAgents for dermatitis, excluding corticosteroidsoclacitinibAuthorisation detailsEMA product number EMEA/V/C/006117 Assessment historyInitial marketing authorisation documentsCVMP summary of positive opinion for ProlevareAdoptedReference Number: EMA/CVMP/66932/2023 English (EN) (125.26 KB - PDF)First published: 17/02/2023ViewNews on ProlevareMeeting highlights from the Committee for Veterinary Medicinal Products (CVMP) 14-16 February 202317/02/2023This page was last updated on 15/02/2024Share this pageHow useful do you find this page?12345