PUREGON 600 UI/0,72 ML SOLUCION INYECTABLE
PUREGON 600 UI/0,72 ML SOLUCION INYECTABLE
Commercialized
Register Number
96008039
Prescription Type
Diagnóstico Hospitalario
Authorization Date
Oct 1, 2000
Dosage Form
SOLUCIÓN INYECTABLE EN CARTUCHO
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 Number96008039
EMA Approved
Yes
Drug Classification
✗
Generic
No
✗
Orphan
No
✗
Biosimilar
No
✓
Commercialized
Yes
CIMA AEMPS Classification
INGREDIENTS (1)
FOLITROPINA BETAActive
Quantity: 833 UI
Name: FOLITROPINA BETA
ATC CLASSIFICATION (3)
G03G
G03GA
G03GA06