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SPEXOTRAS 0,05 MG/ML POLVO PARA SOLUCION ORAL - CIMA-AEMPS Drug Approval Details
Approvals
/
CIMA-AEMPS
/
SPEXOTRAS 0,05 MG/ML POLVO PARA SOLUCION ORAL
Approved
STANDARD
SPEXOTRAS 0,05 MG/ML POLVO PARA SOLUCION ORAL
Novartis Europharm Limited
🇪🇸 Spanish Agency of Medicines and Medical Devices
Approval Date
Apr 10, 2024
Approval ID
3f5616675faf5d73
Company
Novartis Europharm Limited
Type
Standard
Approval Details
Approval Id
3f5616675faf5d73
Drug Cima Aemps Name
SPEXOTRAS 0,05 MG/ML POLVO PARA SOLUCION ORAL
Register Number
1231781001
Holder Company Name
Novartis Europharm Limited
Marketing Company Name
Novartis Farmaceutica S.A.
Holder Company Detail Path
/organization/novartis-europharm-limited
Authorization Date
2024-04-10
Dosage Form
POLVO PARA SOLUCIÓN ORAL
Dose
4,7 mg
Route Of Administration
VÍA ORAL
Prescription Type
Diagnóstico Hospitalario
Commercialized
Yes
Company Name
Novartis Europharm Limited
Company Detail Path
/organization/novartis-europharm-limited
Company Information
Pharmaceutical Company Name
NOVARTIS EUROPHARM LIMITED
Country Name
United Kingdom
City Name
camberley,country_gb
Address
200 Frimley Business Park
Active Ingredients
TRAMETINIB DIMETIL SULFOXIDO
5,3 mg
Approved
Quick Info
Agency
CIMA-AEMPS
Country
🇪🇸
Approval Date
Apr 10, 2024
Approval ID
3f5616675faf5d73
Type
Standard
Back to CIMA-AEMPS Approvals
