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Blincyto



Amgen Europe B.V.EU/1/15/1047/001

Main Information

Trade NameBlincyto
Active SubstancesBlinatumomab
Dosage FormPowder for concentrate and solution for solution for infusion
Licence HolderAmgen Europe B.V.
Licence NumberEU/1/15/1047/001

Group Information

ATC CodeL01XC19 ZZZ Blinatumomab

Status

License statusAuthorised
Licence Issued23/11/2015
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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