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AMGEVITA 40 MG SOLUCION INYECTABLE EN PLUMA PRECARGADA - CIMA-AEMPS Drug Approval Details
Approvals
/
CIMA-AEMPS
/
AMGEVITA 40 MG SOLUCION INYECTABLE EN PLUMA PRECARGADA
Approved
STANDARD
AMGEVITA 40 MG SOLUCION INYECTABLE EN PLUMA PRECARGADA
Amgen Europe B.V.
🇪🇸 Spanish Agency of Medicines and Medical Devices
Approval Date
Jun 7, 2024
Approval ID
5999771c2d3cf4b5
Company
Amgen Europe B.V.
Type
Standard
Approval Details
Approval Id
5999771c2d3cf4b5
Drug Cima Aemps Name
AMGEVITA 40 MG SOLUCION INYECTABLE EN PLUMA PRECARGADA
Register Number
1161164015
Holder Company Name
Amgen Europe B.V.
Marketing Company Name
Amgen S.A.
Holder Company Detail Path
/organization/amgen-europe-b-v
Marketing Company Detail Path
/organization/amgen-sa
Authorization Date
2024-06-07
Dosage Form
SOLUCIÓN INYECTABLE
Dose
40 mg
Route Of Administration
VÍA SUBCUTÁNEA
Prescription Type
Diagnóstico Hospitalario
Commercialized
Yes
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
Active Ingredients
ADALIMUMAB
40 mg
Approved
Quick Info
Agency
CIMA-AEMPS
Country
🇪🇸
Approval Date
Jun 7, 2024
Approval ID
5999771c2d3cf4b5
Type
Standard
Back to CIMA-AEMPS Approvals