Code | 46112 | ||||||||||
MA number | EU/1/98/065/002 | ||||||||||
Product Form: | dis inj 5x3 ml (liek.inj.skl.) | ||||||||||
MA Status: | E - Valid centralised marketing authorisation | ||||||||||
Type of procedure: | EU | ||||||||||
MAH, country: | GE Healthcare AS, Norway | ||||||||||
Therapeutic Class: | 48 - DIAGNOSTICA | ||||||||||
ATC: |
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Shelf life: | 24 | ||||||||||
Container: | glass container | ||||||||||
Route of admin.: | Intravenous use |
Prescription Status: | Medicinal product subject to restricted medical prescription. |
Legal basis: | Article 8(3) application |
MA issued: | 18.05.1998 |
SmPC + PL: | European Medicines Agency's database |
Safety feature | No |
Data update: | 28.10.2019 |