FDA — authorised 17 April 1998
- Application: NDA020819
- Marketing authorisation holder: ABBVIE
- Local brand name: ZEMPLAR
- Indication: SOLUTION — INTRAVENOUS
- Status: approved
FDA authorised Paricalitol on 17 April 1998
Yes. FDA authorised it on 17 April 1998.
ABBVIE holds the US marketing authorisation.