NEUPRO 2, 4, 6, 8 MG/24 H PARCHE TRANSDERMICO
NEUPRO 2, 4, 6, 8 MG/24 H PARCHE TRANSDERMICO
Pending
Register Number
05331013
Prescription Type
Medicamento Sujeto A Prescripción Médica
Authorization Date
Jun 27, 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 Number05331013
EMA Approved
Yes
Drug Classification
✗
Generic
No
✗
Orphan
No
✗
Biosimilar
No
✗
Commercialized
No
CIMA AEMPS Classification
INGREDIENTS (1)
ROTIGOTINAActive
Quantity: 0,45 mg
Name: ROTIGOTINA
ATC CLASSIFICATION (3)
N04B
N04BC
N04BC09