ORUDIS 100 mg SOLUCION INYECTABLE
ORUDIS 100 mg SOLUCION INYECTABLE
Pending
Register Number
55857
Prescription Type
Medicamento Sujeto A Prescripción Médica
Authorization Date
Jun 30, 1982
Dosage Form
SOLUCIÓN INYECTABLE
Route: VÍA INTRAMUSCULAR
Product Details
Detailed information about this CIMA AEMPS approved pharmaceutical product.
Basic Information
Key regulatory and product classification details
Regulatory Details
Register Number55857
EMA Approved
No
Drug Classification
✗
Generic
No
✗
Orphan
No
✗
Biosimilar
No
✗
Commercialized
No
CIMA AEMPS Classification
INGREDIENTS (1)
KETOPROFENOActive
Quantity: 100 mg
Name: KETOPROFENO
ATC CLASSIFICATION (3)
M01A
M01AE
M01AE03