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JEMPERLI 500 MG CONCENTRADO PARA SOLUCION PARA PERFUSION - CIMA-AEMPS Drug Approval Details
Approvals
/
CIMA-AEMPS
/
JEMPERLI 500 MG CONCENTRADO PARA SOLUCION PARA PERFUSION
Approved
STANDARD
JEMPERLI 500 MG CONCENTRADO PARA SOLUCION PARA PERFUSION
Glaxosmithkline (Ireland) Limited
🇪🇸 Spanish Agency of Medicines and Medical Devices
Approval Date
Aug 8, 2025
Approval ID
172b02a2e1b5693e
Company
Glaxosmithkline (Ireland) Limited
Type
Standard
Approval Details
Approval Id
172b02a2e1b5693e
Drug Cima Aemps Name
JEMPERLI 500 MG CONCENTRADO PARA SOLUCION PARA PERFUSION
Register Number
1211538001IP
Holder Company Name
Glaxosmithkline (Ireland) Limited
Marketing Company Name
Abacus Medicine A/S
Holder Company Detail Path
/organization/glaxosmithkline-ireland-limited
Authorization Date
2025-08-08
Dosage Form
CONCENTRADO PARA SOLUCIÓN PARA PERFUSIÓN
Dose
500 mg
Route Of Administration
VÍA INTRAVENOSA
Prescription Type
Uso Hospitalario
Commercialized
Yes
Company Name
Glaxosmithkline (Ireland) Limited
Company Detail Path
/organization/glaxosmithkline-ireland-limited
Company Information
Pharmaceutical Company Name
GLAXOSMITHKLINE (IRELAND) LIMITED
Country Name
Ireland
City Name
dublin,country_ie
Address
12 RIVERWALK
Approved
Quick Info
Agency
CIMA-AEMPS
Country
🇪🇸
Approval Date
Aug 8, 2025
Approval ID
172b02a2e1b5693e
Type
Standard
Back to CIMA-AEMPS Approvals