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Beovu



Novartis Europharm LimitedEU/1/19/1417/001-002

Main Information

Trade NameBeovu
Active SubstancesBrolucizumab
Dosage FormSolution for injection
Licence HolderNovartis Europharm Limited
Licence NumberEU/1/19/1417/001-002

Group Information

ATC CodeS01LA06 brolucizumab

Status

License statusAuthorised
Licence Issued13/02/2020
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

Educational Materials - Patient

Patient Information Guide
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