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KYPROLIS 10 MG POLVO PARA SOLUCION PARA PERFUSION - CIMA-AEMPS Drug Approval Details
Approvals
/
CIMA-AEMPS
/
KYPROLIS 10 MG POLVO PARA SOLUCION PARA PERFUSION
Approved
STANDARD
KYPROLIS 10 MG POLVO PARA SOLUCION PARA PERFUSION
Amgen Europe B.V.
🇪🇸 Spanish Agency of Medicines and Medical Devices
Approval Date
Sep 9, 2025
Approval ID
1cf5ee1ab9d1d9b5
Company
Amgen Europe B.V.
Type
Standard
Approval Details
Approval Id
1cf5ee1ab9d1d9b5
Drug Cima Aemps Name
KYPROLIS 10 MG POLVO PARA SOLUCION PARA PERFUSION
Register Number
1151060002IP1
Holder Company Name
Amgen Europe B.V.
Marketing Company Name
Orifarm A/S
Holder Company Detail Path
/organization/amgen-europe-b-v
Authorization Date
2025-09-09
Dosage Form
POLVO PARA SOLUCIÓN INYECTABLE
Dose
10 mg
Route Of Administration
VÍA INTRAVENOSA
Prescription Type
Uso Hospitalario
Commercialized
No
Company Name
Amgen Europe B.V.
Company Detail Path
/organization/amgen-europe-b-v
Company Information
Pharmaceutical Company Name
AMGEN EUROPE B.V.
Country Name
Israel
City Name
tel aviv-jaffa,central district,country_il
Address
Simtat Maoz
Approved
Quick Info
Agency
CIMA-AEMPS
Country
🇪🇸
Approval Date
Sep 9, 2025
Approval ID
1cf5ee1ab9d1d9b5
Type
Standard
Back to CIMA-AEMPS Approvals
