FDA — authorised 21 November 2017
- Application: NDA210192
- Marketing authorisation holder: VIIV HLTHCARE
- Local brand name: JULUCA
- Indication: TABLET — ORAL
- Status: approved
FDA authorised JULUCA on 21 November 2017
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 21 November 2017.
VIIV HLTHCARE holds the US marketing authorisation.