Code | 36544 | ||||||||||
MA number | EU/1/06/350/001 | ||||||||||
Product Form: | plc fol 10x500 mg+3x500 ml (powder-skl.liek.+diluent-vak PP/PA/PE) | ||||||||||
MA Status: | E - Valid centralised marketing authorisation | ||||||||||
Type of procedure: | EU | ||||||||||
MAH, country: | CNX Therapeutics Ireland Limited, Ireland | ||||||||||
Therapeutic Class: | 87 - VARIA I | ||||||||||
ATC: |
|
||||||||||
Shelf life: | 36 | ||||||||||
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: | 28.07.2006 |
SmPC + PL: | European Medicines Agency's database |
Safety feature | Yes |
Data update: | 19.06.2018 |