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REFIXIA 3000 UI POLVO Y DISOLVENTE PARA SOLUCION INYECTABLE - CIMA-AEMPS Drug Approval Details
Approvals
/
CIMA-AEMPS
/
REFIXIA 3000 UI POLVO Y DISOLVENTE PARA SOLUCION INYECTABLE
Approved
STANDARD
REFIXIA 3000 UI POLVO Y DISOLVENTE PARA SOLUCION INYECTABLE
Novo Nordisk A/S
🇪🇸 Spanish Agency of Medicines and Medical Devices
Approval Date
Mar 23, 2023
Approval ID
7f82bf9031e64e15
Company
Novo Nordisk A/S
Type
Standard
Approval Details
Approval Id
7f82bf9031e64e15
Drug Cima Aemps Name
REFIXIA 3000 UI POLVO Y DISOLVENTE PARA SOLUCION INYECTABLE
Register Number
1171193004
Holder Company Name
Novo Nordisk A/S
Marketing Company Name
Novo Nordisk Pharma S.A.
Holder Company Detail Path
/organization/novo-nordisk-a-s
Authorization Date
2023-03-23
Dosage Form
POLVO Y DISOLVENTE PARA SOLUCIÓN INYECTABLE
Dose
3000 IU
Route Of Administration
VÍA INTRAVENOSA
Prescription Type
Uso Hospitalario
Commercialized
Yes
Company Name
Novo Nordisk A/S
Company Detail Path
/organization/novo-nordisk-a-s
Company Information
Pharmaceutical Company Name
Novo Nordisk A/S
Name En
Novo Nordisk A/S
Country Name
Denmark
City Name
bagsværd,hovedstaden,country_dk
Address
Novo Alle 1
Website
https://www.novonordisk.com
Active Ingredients
NONACOG BETA PEGOL
750 UI/ml
Approved
Quick Info
Agency
CIMA-AEMPS
Country
🇪🇸
Approval Date
Mar 23, 2023
Approval ID
7f82bf9031e64e15
Type
Standard
Back to CIMA-AEMPS Approvals