FDA — authorised 27 April 2007
- Application: NDA022051
- Marketing authorisation holder: HALEON US HOLDINGS
- Local brand name: FLONASE SENSIMIST ALLERGY RELIEF
- Indication: SPRAY, METERED — NASAL
- Status: approved
FDA authorised Fluticasone Furoate (FF) on 27 April 2007
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 27 April 2007.
HALEON US HOLDINGS holds the US marketing authorisation.