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ARMISARTE 25 MG/ML CONCENTRADO PARA SOLUCION PARA PERFUSION - CIMA-AEMPS Drug Approval Details
Approvals
/
CIMA-AEMPS
/
ARMISARTE 25 MG/ML CONCENTRADO PARA SOLUCION PARA PERFUSION
Approved
STANDARD
ARMISARTE 25 MG/ML CONCENTRADO PARA SOLUCION PARA PERFUSION
Actavis Group Ptc Ehf.
🇪🇸 Spanish Agency of Medicines and Medical Devices
Approval Date
Jan 19, 2021
Approval ID
53c36af9dead8d96
Company
Actavis Group Ptc Ehf.
Type
Standard
Approval Details
Approval Id
53c36af9dead8d96
Drug Cima Aemps Name
ARMISARTE 25 MG/ML CONCENTRADO PARA SOLUCION PARA PERFUSION
Register Number
1151063004
Holder Company Name
Actavis Group Ptc Ehf.
Marketing Company Name
Teva Pharma S.L.U.
Holder Company Detail Path
/organization/actavis-group-ptc-ehf
Authorization Date
2021-01-19
Dosage Form
CONCENTRADO PARA SOLUCIÓN PARA PERFUSIÓN
Dose
25 mg/ml
Route Of Administration
VÍA INTRAVENOSA
Prescription Type
Uso Hospitalario
Commercialized
No
Company Name
Actavis Group Ptc Ehf.
Company Detail Path
/organization/actavis-group-ptc-ehf
Company Information
Pharmaceutical Company Name
Actavis Group Ptc Ehf.
Country Name
Norway
City Name
lierskogen,buskerud,country_no
Address
c/o Actavis Norway AS Gjellebekkstubben 10
Active Ingredients
PEMETREXED
25 mg/ml
Approved
Quick Info
Agency
CIMA-AEMPS
Country
🇪🇸
Approval Date
Jan 19, 2021
Approval ID
53c36af9dead8d96
Type
Standard
Back to CIMA-AEMPS Approvals