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RXULTI



Otsuka Pharmaceutical Netherlands B.V.EU/1/18/1294/003-004

Main Information

Trade NameRXULTI
Active SubstancesBREXPIPRAZOLE
Dosage FormFilm-coated tablet
Licence HolderOtsuka Pharmaceutical Netherlands B.V.
Licence NumberEU/1/18/1294/003-004

Group Information

ATC CodeN05AX16 brepiprazole

Status

License statusAuthorised
Licence Issued26/07/2018
Legal statusProduct subject to prescription which may not be renewed (A)
Supply StatusSupply through pharmacies only
Advertising StatusAdvertising to healthcare professionals only
Conditions of Licence
Marketing StatusUnknown

Documents

Summary of Product CharacteristicsSearch EMA website
Package LeafletSearch EMA website
Public Assessment ReportSearch EMA website
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