AZACITIDINA GLENMARK 25 MG/ML POLVO PARA SUSPENSION INYECTABLE EFG
AZACITIDINA GLENMARK 25 MG/ML POLVO PARA SUSPENSION INYECTABLE EFG
Pending
Register Number
86332
Prescription Type
Uso Hospitalario
Authorization Date
Oct 22, 2021
Dosage Form
POLVO PARA SUSPENSIÓN 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 Number86332
EMA Approved
No
Drug Classification
✓
Generic
Yes
✗
Orphan
No
✗
Biosimilar
No
✗
Commercialized
No
CIMA AEMPS Classification
INGREDIENTS (1)
AZACITIDINAActive
Quantity: 25 mg/ml
Name: AZACITIDINA
ATC CLASSIFICATION (3)
L01B
L01BC
L01BC07