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RYBREVANT 1600 MG SOLUCION INYECTABLE - CIMA-AEMPS Drug Approval Details
Approvals
/
CIMA-AEMPS
/
RYBREVANT 1600 MG SOLUCION INYECTABLE
Approved
STANDARD
RYBREVANT 1600 MG SOLUCION INYECTABLE
Janssen-Cilag International N.V
🇪🇸 Spanish Agency of Medicines and Medical Devices
Approval Date
Apr 14, 2025
Approval ID
2143c1b818b78590
Company
Janssen-Cilag International N.V
Type
Standard
Approval Details
Approval Id
2143c1b818b78590
Drug Cima Aemps Name
RYBREVANT 1600 MG SOLUCION INYECTABLE
Register Number
1211594002
Holder Company Name
Janssen-Cilag International N.V
Marketing Company Name
Janssen Cilag S.A.
Holder Company Detail Path
/organization/janssen-cilag-international-nv
Authorization Date
2025-04-14
Dosage Form
SOLUCIÓN INYECTABLE
Dose
1600 mg
Route Of Administration
VÍA SUBCUTÁNEA
Prescription Type
Uso Hospitalario
Commercialized
Yes
Company Name
Janssen-Cilag International N.V
Company Detail Path
/organization/janssen-cilag-international-nv
Company Information
Pharmaceutical Company Name
Janssen-Cilag International NV
Country Name
Belgium
Active Ingredients
AMIVANTAMAB
1600 mg
Approved
Quick Info
Agency
CIMA-AEMPS
Country
🇪🇸
Approval Date
Apr 14, 2025
Approval ID
2143c1b818b78590
Type
Standard
Back to CIMA-AEMPS Approvals