NEORECORMON 20000 UI LIOFILIZADO Y DISOLVENTE PARA SOLUCION INYECTABLE EN CARTUCHO
NEORECORMON 20000 UI LIOFILIZADO Y DISOLVENTE PARA SOLUCION INYECTABLE EN CARTUCHO
Pending
Register Number
97031024
Prescription Type
Uso Hospitalario
Authorization Date
Oct 31, 1997
Dosage Form
POLVO Y DISOLVENTE PARA SOLUCIÓN INYECTABLE Y PARA PERFUSIÓN
Route: VÍA INTRAVENOSA
Product Details
Detailed information about this CIMA AEMPS approved pharmaceutical product.
Basic Information
Key regulatory and product classification details
Regulatory Details
Register Number97031024
EMA Approved
Yes
Drug Classification
✗
Generic
No
✗
Orphan
No
✗
Biosimilar
No
✗
Commercialized
No
CIMA AEMPS Classification
INGREDIENTS (1)
EPOETINA BETAActive
Quantity: 20 kilo UI
Name: EPOETINA BETA
ATC CLASSIFICATION (3)
B03X
B03XA
B03XA01