PLERIXAFOR GLENMARK 20 MG/ML SOLUCION INYECTABLE EFG
PLERIXAFOR GLENMARK 20 MG/ML SOLUCION INYECTABLE EFG
Commercialized
Register Number
88904
Prescription Type
Uso Hospitalario
Authorization Date
Jun 14, 2023
Dosage Form
SOLUCIÓN INYECTABLE
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 Number88904
EMA Approved
No
Drug Classification
✓
Generic
Yes
✗
Orphan
No
✗
Biosimilar
No
✓
Commercialized
Yes
CIMA AEMPS Classification
INGREDIENTS (1)
PLERIXAFORActive
Quantity: 20 mg
Name: PLERIXAFOR
ATC CLASSIFICATION (3)
L03A
L03AX
L03AX16