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BUPROPION SUN 150 MG COMPRIMIDOS DE LIBERACION MODIFICADA EFG - CIMA-AEMPS Drug Approval Details
Approvals
/
CIMA-AEMPS
/
BUPROPION SUN 150 MG COMPRIMIDOS DE LIBERACION MODIFICADA EFG
Approved
STANDARD
BUPROPION SUN 150 MG COMPRIMIDOS DE LIBERACION MODIFICADA EFG
Sun Pharmaceutical Industries (Europe) B.V.
🇪🇸 Spanish Agency of Medicines and Medical Devices
Approval Date
Jan 20, 2025
Approval ID
e6f3ebc2f5344e27
Company
Sun Pharmaceutical Industries (Europe) B.V.
Type
Standard
Approval Details
Approval Id
e6f3ebc2f5344e27
Drug Cima Aemps Name
BUPROPION SUN 150 MG COMPRIMIDOS DE LIBERACION MODIFICADA EFG
Register Number
90083
Holder Company Name
Sun Pharmaceutical Industries (Europe) B.V.
Marketing Company Name
Sun Pharma Laboratorios S.L.
Holder Company Detail Path
/organization/sun-pharmaceutical-industries-europe-b-v
Authorization Date
2025-01-20
Dosage Form
COMPRIMIDO DE LIBERACIÓN MODIFICADA
Dose
150 mg
Route Of Administration
VÍA ORAL
Prescription Type
Medicamento Sujeto A Prescripción Médica
Commercialized
No
Company Name
Sun Pharmaceutical Industries (Europe) B.V.
Company Detail Path
/organization/sun-pharmaceutical-industries-europe-b-v
Company Information
Pharmaceutical Company Name
Sun Pharmaceutical Industries (Europe) B.V.
Country Name
Netherlands
City Name
hoofddorp,noord-holland,country_nl
Address
Polarisavenue 87
Active Ingredients
BUPROPION HIDROCLORURO
150 mg
Approved
Quick Info
Agency
CIMA-AEMPS
Country
🇪🇸
Approval Date
Jan 20, 2025
Approval ID
e6f3ebc2f5344e27
Type
Standard
Back to CIMA-AEMPS Approvals