The European Commission has granted a marketing authorization for Stada and Xbrane Biopharma’s Ximluci (ranibizumab) 10mg/ml solution for injection biosimilar rival to Lucentis. The authorization covers all 27 EU member states as well as Iceland, Norway, and Lichtenstein.
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Generics Bulletin for daily insights
- Start your 7-day free trial
- Explore trusted news, analysis, and insights
- Access comprehensive global coverage
- Enjoy instant access – no credit card required
Already a subscriber?