🇺🇸 Tenofovir DF in United States

FDA authorised Tenofovir DF on 26 October 2001

Marketing authorisations

FDA — authorised 26 October 2001

  • Application: NDA021356
  • Marketing authorisation holder: GILEAD SCIENCES INC
  • Local brand name: VIREAD
  • Indication: TABLET — ORAL
  • Status: approved

Read official source →

FDA — authorised 18 January 2012

  • Application: NDA022577
  • Marketing authorisation holder: GILEAD SCIENCES INC
  • Local brand name: VIREAD
  • Indication: POWDER — ORAL
  • Status: approved

Read official source →

FDA

  • Status: approved

Tenofovir DF in other countries

Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.

Frequently asked questions

Is Tenofovir DF approved in United States?

Yes. FDA authorised it on 26 October 2001; FDA authorised it on 18 January 2012; FDA has authorised it.

Who is the marketing authorisation holder for Tenofovir DF in United States?

GILEAD SCIENCES INC holds the US marketing authorisation.