FDA — authorised 8 October 2008
- Application: NDA022206
- Marketing authorisation holder: ABBVIE
- Local brand name: RAPAFLO
- Indication: CAPSULE — ORAL
- Status: approved
FDA authorised Preventive administration of Rapaflo on 8 October 2008
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 8 October 2008; FDA authorised it on 31 March 2017; FDA authorised it on 3 December 2018.
ABBVIE holds the US marketing authorisation.