FDA — authorised 12 April 2000
- Application: NDA021119
- Marketing authorisation holder: BAUSCH LOMB IRELAND
- Local brand name: VISUDYNE
- Indication: INJECTABLE — INJECTION
- Status: approved
FDA authorised Visudyne on 12 April 2000
Yes. FDA authorised it on 12 April 2000.
BAUSCH LOMB IRELAND holds the US marketing authorisation.