FDA — authorised 17 April 1998
- Application: NDA020819
- Marketing authorisation holder: ABBVIE
- Status: supplemented
FDA authorised Zemplar on 17 April 1998
Yes. FDA authorised it on 17 April 1998; FDA authorised it on 26 May 2005; FDA has authorised it.
ABBVIE holds the US marketing authorisation.