FDA — authorised 30 August 2018
- Application: NDA210807
- Marketing authorisation holder: MSD MERCK CO
- Local brand name: DELSTRIGO
- Indication: TABLET — ORAL
- Status: approved
FDA authorised Doravirine + tenofovir DF + lamivudine on 30 August 2018
Yes. FDA authorised it on 30 August 2018.
MSD MERCK CO holds the US marketing authorisation.