FDA — authorised 31 October 2000
- Application: NDA021183
- Marketing authorisation holder: BRISTOL MYERS SQUIBB
- Local brand name: VIDEX EC
- Indication: CAPSULE, DELAYED REL PELLETS — ORAL
- Status: approved
🇺🇸 Videx EC in United States
FDA authorised Videx EC on 31 October 2000
Marketing authorisation
Other Infectious Disease / Virology approved in United States
Frequently asked questions
Is Videx EC approved in United States?
Yes. FDA authorised it on 31 October 2000.
Who is the marketing authorisation holder for Videx EC in United States?
BRISTOL MYERS SQUIBB holds the US marketing authorisation.