🇺🇸 Doravirine + tenofovir DF + lamivudine in United States

FDA authorised Doravirine + tenofovir DF + lamivudine on 30 August 2018

Marketing authorisation

FDA — authorised 30 August 2018

  • Application: NDA210807
  • Marketing authorisation holder: MSD MERCK CO
  • Local brand name: DELSTRIGO
  • Indication: TABLET — ORAL
  • Status: approved

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Other Infectious Disease / Virology approved in United States

Frequently asked questions

Is Doravirine + tenofovir DF + lamivudine approved in United States?

Yes. FDA authorised it on 30 August 2018.

Who is the marketing authorisation holder for Doravirine + tenofovir DF + lamivudine in United States?

MSD MERCK CO holds the US marketing authorisation.