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NEPARVIS 49 MG/51 MG COMPRIMIDOS RECUBIERTOS CON PELICULA - CIMA-AEMPS Drug Approval Details
Approvals
/
CIMA-AEMPS
/
NEPARVIS 49 MG/51 MG COMPRIMIDOS RECUBIERTOS CON PELICULA
Approved
STANDARD
NEPARVIS 49 MG/51 MG COMPRIMIDOS RECUBIERTOS CON PELICULA
Novartis Europharm Limited
🇪🇸 Spanish Agency of Medicines and Medical Devices
Approval Date
Nov 15, 2022
Approval ID
6693fd507b3cd048
Company
Novartis Europharm Limited
Type
Standard
Approval Details
Approval Id
6693fd507b3cd048
Drug Cima Aemps Name
NEPARVIS 49 MG/51 MG COMPRIMIDOS RECUBIERTOS CON PELICULA
Register Number
161103003IP
Holder Company Name
Novartis Europharm Limited
Marketing Company Name
Melyfarma S.L.
Holder Company Detail Path
/organization/novartis-europharm-limited
Authorization Date
2022-11-15
Dosage Form
COMPRIMIDO RECUBIERTO CON PELÍCULA
Dose
49 mg/51 mg
Route Of Administration
VÍA ORAL
Prescription Type
Medicamento Sujeto A Prescripción Médica
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
SACUBITRILO
48,6 mg
VALSARTAN
51,4 mg
Approved
Quick Info
Agency
CIMA-AEMPS
Country
🇪🇸
Approval Date
Nov 15, 2022
Approval ID
6693fd507b3cd048
Type
Standard
Back to CIMA-AEMPS Approvals