MedPath

DUODOPA 240 MG/ML + 12 MG/ML SOLUCION PARA PERFUSION

DUODOPA 240 MG/ML + 12 MG/ML SOLUCION PARA PERFUSION

Commercialized
Register Number

88677

Prescription Type

Uso Hospitalario

Authorization Date

Feb 20, 2023

Dosage Form

SOLUCIÓN PARA PERFUSIÓN

Route: VÍA SUBCUTÁNEA

Product Details

Detailed information about this CIMA AEMPS approved pharmaceutical product.

Basic Information

Key regulatory and product classification details

Regulatory Details

Register Number88677
EMA Approved
No

Drug Classification

Generic
No
Orphan
No
Biosimilar
No
Commercialized
Yes
CIMA AEMPS Classification

INGREDIENTS (2)

FOSCARBIDOPAActive
Quantity: 12 mg
Name: FOSCARBIDOPA
FOSLEVODOPAActive
Quantity: 240 mg/ml
Name: FOSLEVODOPA

ATC CLASSIFICATION (3)

N04B
N04BA
N04BA07

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.