Code | 7211A | ||||||||||
MA number | EU/1/13/869/001 | ||||||||||
Product Form: | con inf 1x1,2 ml/12 mg (liek.inj.skl.) | ||||||||||
MA Status: | E - Valid centralised marketing authorisation | ||||||||||
Type of procedure: | EU | ||||||||||
MAH, country: | Sanofi Belgium, Belgium | ||||||||||
Therapeutic Class: | 59 - IMMUNOPRAEPARATA | ||||||||||
ATC: |
|
||||||||||
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 - known active substance |
MA issued: | 12.09.2013 |
SmPC + PL: |
|
Safety feature | Yes |
Data update: | 14.07.2023 |