FDA — authorised 25 February 2015
- Application: BLA206538
- Marketing authorisation holder: SANOFI US SERVICES
- Local brand name: TOUJEO SOLOSTAR
- Indication: SOLUTION — SUBCUTANEOUS
- Status: approved
FDA authorised Toujeo SoloStar on 25 February 2015
Yes. FDA authorised it on 25 February 2015.
SANOFI US SERVICES holds the US marketing authorisation.