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OPDUALAG 240 MG/80 MG CONCENTRADO PARA SOLUCION PARA PERFUSION - CIMA-AEMPS Drug Approval Details
Approvals
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CIMA-AEMPS
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OPDUALAG 240 MG/80 MG CONCENTRADO PARA SOLUCION PARA PERFUSION
Approved
STANDARD
OPDUALAG 240 MG/80 MG CONCENTRADO PARA SOLUCION PARA PERFUSION
Bristol-Myers Squibb Pharma Eeig
🇪🇸 Spanish Agency of Medicines and Medical Devices
Approval Date
Jan 10, 2024
Approval ID
dc9fb700369332c3
Company
Bristol-Myers Squibb Pharma Eeig
Type
Standard
Approval Details
Approval Id
dc9fb700369332c3
Drug Cima Aemps Name
OPDUALAG 240 MG/80 MG CONCENTRADO PARA SOLUCION PARA PERFUSION
Register Number
1221679001
Holder Company Name
Bristol-Myers Squibb Pharma Eeig
Marketing Company Name
Bristol Myers Squibb S.A.
Holder Company Detail Path
/organization/bristol-myers-squibb-pharma-eeig
Authorization Date
2024-01-10
Dosage Form
CONCENTRADO PARA SOLUCIÓN PARA PERFUSIÓN
Dose
240 mg/80 mg
Route Of Administration
VÍA INTRAVENOSA
Prescription Type
Uso Hospitalario
Commercialized
No
Company Name
Bristol-Myers Squibb Pharma Eeig
Company Detail Path
/organization/bristol-myers-squibb-pharma-eeig
Company Information
Pharmaceutical Company Name
Bristol-Myers Squibb Pharma EEIG
Country Name
Ireland
Active Ingredients
RELATLIMAB
85,20 mg
NIVOLUMAB
255,60 mg
Approved
Quick Info
Agency
CIMA-AEMPS
Country
🇪🇸
Approval Date
Jan 10, 2024
Approval ID
dc9fb700369332c3
Type
Standard
Back to CIMA-AEMPS Approvals