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BORTEZOMIB SUN 3,5 MG POLVO PARA SOLUCION INYECTABLE EFG - CIMA-AEMPS Drug Approval Details
Approvals
/
CIMA-AEMPS
/
BORTEZOMIB SUN 3,5 MG POLVO PARA SOLUCION INYECTABLE EFG
Approved
STANDARD
BORTEZOMIB SUN 3,5 MG POLVO PARA SOLUCION INYECTABLE EFG
Sun Pharmaceutical Industries (Europe) B.V.
🇪🇸 Spanish Agency of Medicines and Medical Devices
Approval Date
Nov 4, 2020
Approval ID
938a0ba0da78ffc6
Company
Sun Pharmaceutical Industries (Europe) B.V.
Type
Standard
Approval Details
Approval Id
938a0ba0da78ffc6
Drug Cima Aemps Name
BORTEZOMIB SUN 3,5 MG POLVO PARA SOLUCION INYECTABLE EFG
Register Number
1161102001
Holder Company Name
Sun Pharmaceutical Industries (Europe) B.V.
Marketing Company Name
Sun Pharma Laboratorios S.L.
Holder Company Detail Path
/organization/sun-pharmaceutical-industries-europe-b-v
Authorization Date
2020-11-04
Dosage Form
POLVO PARA SOLUCIÓN INYECTABLE
Dose
3,5 mg
Route Of Administration
VÍA INTRAVENOSA, VÍA SUBCUTÁNEA
Prescription Type
Uso Hospitalario
Commercialized
Yes
Company Name
Sun Pharmaceutical Industries (Europe) B.V.
Company Detail Path
/organization/sun-pharmaceutical-industries-europe-b-v
Company Information
Pharmaceutical Company Name
Sun Pharmaceutical Industries (Europe) B.V.
Country Name
Netherlands
City Name
hoofddorp,noord-holland,country_nl
Address
Polarisavenue 87
Active Ingredients
BORTEZOMIB
3,5 mg
Approved
Quick Info
Agency
CIMA-AEMPS
Country
🇪🇸
Approval Date
Nov 4, 2020
Approval ID
938a0ba0da78ffc6
Type
Standard
Back to CIMA-AEMPS Approvals