FDA — authorised 29 October 2004
- Application: NDA021457
- Marketing authorisation holder: TEVA BRANDED PHARM
- Local brand name: PROAIR HFA
- Indication: AEROSOL, METERED — INHALATION
- Status: approved
🇺🇸 ProAir® HFA in United States
FDA authorised ProAir® HFA on 29 October 2004
Marketing authorisation
Other Respiratory / Pulmonology approved in United States
Frequently asked questions
Is ProAir® HFA approved in United States?
Yes. FDA authorised it on 29 October 2004.
Who is the marketing authorisation holder for ProAir® HFA in United States?
TEVA BRANDED PHARM holds the US marketing authorisation.