EMA — authorised 31 December 2009
- Application: EMEA/H/C/000801
- Marketing authorisation holder: Guerbet
- Local brand name: Sinerem
- Status: withdrawn
EMA authorised Iron Oxide on 31 December 2009
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. EMA authorised it on 31 December 2009.
Guerbet holds the EU marketing authorisation.