ORUDIS 50 mg CAPSULAS
ORUDIS 50 mg CAPSULAS
Pending
Register Number
52097
Prescription Type
Medicamento Sujeto A Prescripción Médica
Authorization Date
Jan 31, 1974
Dosage Form
CÁPSULA DURA
Route: VÍA ORAL
Product Details
Detailed information about this CIMA AEMPS approved pharmaceutical product.
Basic Information
Key regulatory and product classification details
Regulatory Details
Register Number52097
EMA Approved
No
Drug Classification
✗
Generic
No
✗
Orphan
No
✗
Biosimilar
No
✗
Commercialized
No
CIMA AEMPS Classification
INGREDIENTS (1)
KETOPROFENOActive
Quantity: 50 mg
Name: KETOPROFENO
ATC CLASSIFICATION (3)
M01A
M01AE
M01AE03