FDA — authorised 23 February 2007
- Application: NDA021977
- Marketing authorisation holder: TAKEDA PHARMS USA
- Status: supplemented
FDA authorised Vyvanse on 23 February 2007
Yes. FDA authorised it on 23 February 2007; FDA authorised it on 28 January 2017; FDA has authorised it.
TAKEDA PHARMS USA holds the US marketing authorisation.