FDA — authorised 16 February 2001
- Application: NDA020831
- Marketing authorisation holder: NOVARTIS
- Local brand name: FORADIL
- Indication: POWDER — INHALATION
- Status: approved
🇺🇸 Racemic formoterol in United States
FDA authorised Racemic formoterol on 16 February 2001
Marketing authorisations
FDA — authorised 25 September 2001
- Application: NDA021279
- Marketing authorisation holder: NOVARTIS
- Local brand name: FORADIL
- Indication: POWDER — INHALATION
- Status: approved
Frequently asked questions
Is Racemic formoterol approved in United States?
Yes. FDA authorised it on 16 February 2001; FDA authorised it on 25 September 2001.
Who is the marketing authorisation holder for Racemic formoterol in United States?
NOVARTIS holds the US marketing authorisation.