NEUPRO 8 MG/24 H PARCHE TRANSDERMICO
NEUPRO 8 MG/24 H PARCHE TRANSDERMICO
Commercialized
Register Number
05331011
Prescription Type
Medicamento Sujeto A Prescripción Médica
Authorization Date
Apr 20, 2006
Dosage Form
PARCHE TRANSDÉRMICO
Route: VÍA TRANSDÉRMICA
Product Details
Detailed information about this CIMA AEMPS approved pharmaceutical product.
Basic Information
Key regulatory and product classification details
Regulatory Details
Register Number05331011
EMA Approved
Yes
Drug Classification
✗
Generic
No
✗
Orphan
No
✗
Biosimilar
No
✓
Commercialized
Yes
CIMA AEMPS Classification
INGREDIENTS (1)
ROTIGOTINAActive
Quantity: 8 g
Name: ROTIGOTINA
ATC CLASSIFICATION (3)
N04B
N04BC
N04BC09