EMA — authorised 31 December 2009
- Application: EMEA/H/C/000838
- Marketing authorisation holder: Takeda Global Research Development Centre (Europe) Ltd.
- Local brand name: Ramelteon
- Status: withdrawn
🇪🇺 Ramelteon Pill in European Union
EMA authorised Ramelteon Pill on 31 December 2009
Marketing authorisation
Ramelteon Pill in other countries
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Frequently asked questions
Is Ramelteon Pill approved in European Union?
Yes. EMA authorised it on 31 December 2009.
Who is the marketing authorisation holder for Ramelteon Pill in European Union?
Takeda Global Research Development Centre (Europe) Ltd. holds the EU marketing authorisation.