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ACTONEL SEMANAL 35 MG COMPRIMIDOS RECUBIERTOS CON PELICULA - CIMA-AEMPS Drug Approval Details
Approvals
/
CIMA-AEMPS
/
ACTONEL SEMANAL 35 MG COMPRIMIDOS RECUBIERTOS CON PELICULA
Approved
STANDARD
ACTONEL SEMANAL 35 MG COMPRIMIDOS RECUBIERTOS CON PELICULA
Theramex Ireland Limited
🇪🇸 Spanish Agency of Medicines and Medical Devices
Approval Date
Oct 27, 2023
Approval ID
aff16d462bad916a
Company
Theramex Ireland Limited
Type
Standard
Approval Details
Approval Id
aff16d462bad916a
Drug Cima Aemps Name
ACTONEL SEMANAL 35 MG COMPRIMIDOS RECUBIERTOS CON PELICULA
Register Number
2853-2010-01-06IP
Holder Company Name
Theramex Ireland Limited
Marketing Company Name
Elam Pharma Labs S.L.
Holder Company Detail Path
/organization/theramex-ireland-ltd
Authorization Date
2023-10-27
Dosage Form
COMPRIMIDO RECUBIERTO CON PELÍCULA
Dose
35 mg
Route Of Administration
VÍA ORAL
Prescription Type
Medicamento Sujeto A Prescripción Médica
Commercialized
No
Company Name
Theramex Ireland Limited
Company Detail Path
/organization/theramex-ireland-ltd
Company Information
Pharmaceutical Company Name
Theramex Ireland Ltd.
Country Name
Ireland
Active Ingredients
RISEDRONATO SODIO
35 mg
Approved
Quick Info
Agency
CIMA-AEMPS
Country
🇪🇸
Approval Date
Oct 27, 2023
Approval ID
aff16d462bad916a
Type
Standard
Back to CIMA-AEMPS Approvals