FDA — authorised 20 May 1999
- Application: NDA021042
- Marketing authorisation holder: MERCK
- Local brand name: VIOXX
- Indication: TABLET — ORAL
- Status: approved
FDA authorised Vioxx on 20 May 1999
Yes. FDA authorised it on 20 May 1999; FDA authorised it on 20 May 1999.
MERCK holds the US marketing authorisation.