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AVIDART 0,5 MG CAPSULAS BLANDAS - CIMA-AEMPS Drug Approval Details
Approvals
/
CIMA-AEMPS
/
AVIDART 0,5 MG CAPSULAS BLANDAS
Approved
STANDARD
AVIDART 0,5 MG CAPSULAS BLANDAS
Glaxosmithkline A.E.B.E.
🇪🇸 Spanish Agency of Medicines and Medical Devices
Approval Date
Nov 8, 2023
Approval ID
2537079dd53a517b
Company
Glaxosmithkline A.E.B.E.
Type
Standard
Approval Details
Approval Id
2537079dd53a517b
Drug Cima Aemps Name
AVIDART 0,5 MG CAPSULAS BLANDAS
Register Number
58047-04-09-2015IP
Holder Company Name
Glaxosmithkline A.E.B.E.
Marketing Company Name
Euromed Pharma Spain S.L.
Authorization Date
2023-11-08
Dosage Form
CÁPSULA BLANDA
Dose
0,5 mg
Route Of Administration
VÍA ORAL
Prescription Type
Medicamento Sujeto A Prescripción Médica
Commercialized
Yes
Company Name
Glaxosmithkline A.E.B.E.
Approved
Quick Info
Agency
CIMA-AEMPS
Country
🇪🇸
Approval Date
Nov 8, 2023
Approval ID
2537079dd53a517b
Type
Standard
Back to CIMA-AEMPS Approvals