Code | 1475E | ||||||||||
MA number | EU/1/22/1659/002 | ||||||||||
Product Form: | plc ifc 5x20 mg (liek.inj.skl.) | ||||||||||
MA Status: | E - Valid centralised marketing authorisation | ||||||||||
Type of procedure: | EU Orphan | ||||||||||
MAH, country: | Sanofi B.V., Netherland | ||||||||||
Therapeutic Class: | 87 - VARIA I | ||||||||||
ATC: |
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Shelf life: | 48 | ||||||||||
Container: | glass vial | ||||||||||
Route of admin.: | Intravenous use |
Prescription Status: | Medicinal product subject to restricted medical prescription. |
Legal basis: | Article 8(3) application - new active substance |
MA issued: | 24.06.2022 |
Validity: | 24.06.2027 |
SmPC + PL: |
|
Safety feature | Yes |
Data update: | 23.08.2022 |