Code | 41226 | ||||||||||
MA number | EU/1/01/176/006 | ||||||||||
Product Form: | con inf 10x5 ml/4 mg (liek.inj.plast.) | ||||||||||
MA Status: | E - Valid centralised marketing authorisation | ||||||||||
Type of procedure: | EU | ||||||||||
MAH, country: | Phoenix Labs Unlimited Company, Ireland | ||||||||||
Therapeutic Class: | 87 - VARIA I | ||||||||||
ATC: |
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Shelf life: | 36 | ||||||||||
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: | 20.03.2001 |
SmPC + PL: | European Medicines Agency's database |
Safety feature | Yes |
Data update: | 07.04.2021 |