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Lorviqua



Pfizer Europe MA EEIGEU/1/19/1355/001

Main Information

Trade NameLorviqua
Active SubstancesLORLATINIB
Dosage FormFilm-coated tablet
Licence HolderPfizer Europe MA EEIG
Licence NumberEU/1/19/1355/001

Group Information

ATC CodeL01 ANTINEOPLASTIC AGENTS
L01XE44 lorlatinib

Status

License statusAuthorised
Licence Issued06/05/2019
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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