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Approvals
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CIMA-AEMPS
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SCEMBLIX 20 MG COMPRIMIDOS RECUBIERTOS CON PELICULA
Approved
STANDARD
SCEMBLIX 20 MG COMPRIMIDOS RECUBIERTOS CON PELICULA
Novartis Europharm Limited
🇪🇸 Spanish Agency of Medicines and Medical Devices
Approval Date
Oct 6, 2022
Approval ID
7668a58771bea332
Company
Novartis Europharm Limited
Type
Standard
Approval Details
Approval Id
7668a58771bea332
Drug Cima Aemps Name
SCEMBLIX 20 MG COMPRIMIDOS RECUBIERTOS CON PELICULA
Register Number
1221670002
Holder Company Name
Novartis Europharm Limited
Marketing Company Name
Novartis Farmaceutica S.A.
Holder Company Detail Path
/organization/novartis-europharm-limited
Authorization Date
2022-10-06
Dosage Form
COMPRIMIDO RECUBIERTO CON PELÍCULA
Dose
20 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
ASCIMINIB HIDROCLORURO
21,620 mg
Approved
Quick Info
Agency
CIMA-AEMPS
Country
🇪🇸
Approval Date
Oct 6, 2022
Approval ID
7668a58771bea332
Type
Standard
Back to CIMA-AEMPS Approvals
SCEMBLIX 20 MG COMPRIMIDOS RECUBIERTOS CON PELICULA - CIMA-AEMPS Drug Approval Details
