FDA — authorised 31 March 2015
- Application: NDA205636
- Marketing authorisation holder: TEVA BRANDED PHARM
- Local brand name: PROAIR DIGIHALER
- Indication: POWDER, METERED — INHALATION
- Status: approved
🇺🇸 ProAir Digihaler in United States
FDA authorised ProAir Digihaler on 31 March 2015
Marketing authorisation
Other Respiratory approved in United States
Frequently asked questions
Is ProAir Digihaler approved in United States?
Yes. FDA authorised it on 31 March 2015.
Who is the marketing authorisation holder for ProAir Digihaler in United States?
TEVA BRANDED PHARM holds the US marketing authorisation.