FDA — authorised 22 August 2014
- Application: NDA205551
- Marketing authorisation holder: VIIV HLTHCARE
- Local brand name: TRIUMEQ
- Indication: TABLET — ORAL
- Status: approved
FDA authorised Triumeq on 22 August 2014
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 22 August 2014; FDA authorised it on 30 March 2022; FDA has authorised it.
VIIV HLTHCARE holds the US marketing authorisation.