EMA — authorised 31 December 2009
- Application: EMEA/H/C/000635
- Marketing authorisation holder: Alcon Laboratories (U.K.) Limited.
- Local brand name: Retaane
- Status: withdrawn
🇪🇺 Retaane in European Union
EMA authorised Retaane on 31 December 2009
Marketing authorisation
Retaane in other countries
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Other Ophthalmology approved in European Union
Frequently asked questions
Is Retaane approved in European Union?
Yes. EMA authorised it on 31 December 2009.
Who is the marketing authorisation holder for Retaane in European Union?
Alcon Laboratories (U.K.) Limited. holds the EU marketing authorisation.