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Approvals
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CIMA-AEMPS
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SOLIFENACINA/TAMSULOSINA VIATRIS 6 MG/0,4 MG COMPRIMIDOS DE LIBERACION MODIFICADA EFG
Approved
STANDARD
SOLIFENACINA/TAMSULOSINA VIATRIS 6 MG/0,4 MG COMPRIMIDOS DE LIBERACION MODIFICADA EFG
Viatris Limited
🇪🇸 Spanish Agency of Medicines and Medical Devices
Approval Date
Oct 4, 2023
Approval ID
bc505846af791020
Company
Viatris Limited
Type
Standard
Approval Details
Approval Id
bc505846af791020
Drug Cima Aemps Name
SOLIFENACINA/TAMSULOSINA VIATRIS 6 MG/0,4 MG COMPRIMIDOS DE LIBERACION MODIFICADA EFG
Register Number
89055
Holder Company Name
Viatris Limited
Marketing Company Name
Viatris Pharmaceuticals S.L.U.
Holder Company Detail Path
/organization/viatris-pharma-limited
Authorization Date
2023-10-04
Dosage Form
COMPRIMIDO DE LIBERACIÓN MODIFICADA
Dose
6 mg/0,4 mg
Route Of Administration
VÍA ORAL
Prescription Type
Medicamento Sujeto A Prescripción Médica
Commercialized
Yes
Company Name
Viatris Limited
Company Detail Path
/organization/viatris-pharma-limited
Company Information
Pharmaceutical Company Name
VIATRIS PHARMA LIMITED
Country Name
Hong Kong, China
City Name
sha tin,country_hk
Address
Rm A7 8/F WAH WAI INDL BLDG
Active Ingredients
SOLIFENACINA SUCCINATO
6 mg
TAMSULOSINA HIDROCLORURO
0,4 mg
Approved
Quick Info
Agency
CIMA-AEMPS
Country
🇪🇸
Approval Date
Oct 4, 2023
Approval ID
bc505846af791020
Type
Standard
Back to CIMA-AEMPS Approvals
SOLIFENACINA/TAMSULOSINA VIATRIS 6 MG/0,4 MG COMPRIMIDOS DE LIBERACION MODIFICADA EFG - CIMA-AEMPS Drug Approval Details