跳至主要内容
MedPath Trial Home
临床试验
产品
机构
资讯
AI 研究
价格
Search
EN
登录
我们重视您的隐私
我们使用 Cookie 分析网站流量并改善您的体验。请参阅我们的
隐私政策
。
拒绝
接受
DUODOPA 240 MG/ML + 12 MG/ML SOLUCION PARA PERFUSION - CIMA-AEMPS Drug Approval Details
Approvals
/
CIMA-AEMPS
/
DUODOPA 240 MG/ML + 12 MG/ML SOLUCION PARA PERFUSION
Approved
STANDARD
DUODOPA 240 MG/ML + 12 MG/ML SOLUCION PARA PERFUSION
Abbvie Spain, S.L.U.
🇪🇸 Spanish Agency of Medicines and Medical Devices
Approval Date
Feb 20, 2023
Approval ID
68e35ed888526190
Company
Abbvie Spain, S.L.U.
Type
Standard
Approval Details
Approval Id
68e35ed888526190
Drug Cima Aemps Name
DUODOPA 240 MG/ML + 12 MG/ML SOLUCION PARA PERFUSION
Register Number
88677
Holder Company Name
Abbvie Spain, S.L.U.
Marketing Company Name
Abbvie Spain, S.L.U.
Authorization Date
2023-02-20
Dosage Form
SOLUCIÓN PARA PERFUSIÓN
Dose
240 MG/ML + 12 MG/ML
Route Of Administration
VÍA SUBCUTÁNEA
Prescription Type
Uso Hospitalario
Commercialized
Yes
Company Name
Abbvie Spain, S.L.U.
Active Ingredients
FOSLEVODOPA
240 mg/ml
FOSCARBIDOPA
12 mg
Approved
Quick Info
Agency
CIMA-AEMPS
Country
🇪🇸
Approval Date
Feb 20, 2023
Approval ID
68e35ed888526190
Type
Standard
Back to CIMA-AEMPS Approvals