🇺🇸 Victoza in United States

FDA authorised Victoza on 25 February 2015

Marketing authorisations

FDA — authorised 25 February 2015

  • Application: NDA022341
  • Marketing authorisation holder: NOVO NORDISK INC
  • Indication: Labeling
  • Status: approved

Read official source →

FDA — authorised 2 April 2025

  • Application: ANDA218115
  • Marketing authorisation holder: NANJING KING FRIEND
  • Status: approved

Read official source →

FDA — authorised 27 August 2025

  • Application: ANDA214568
  • Marketing authorisation holder: TEVA PHARMS
  • Status: approved

Read official source →

FDA — authorised 14 January 2026

  • Application: ANDA217590
  • Marketing authorisation holder: ORBICULAR
  • Status: approved

Read official source →

FDA — authorised 24 February 2026

  • Application: ANDA217234
  • Marketing authorisation holder: ORBICULAR
  • Status: approved

Read official source →

Victoza in other countries

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

Other Metabolic approved in United States

Frequently asked questions

Is Victoza approved in United States?

Yes. FDA authorised it on 25 February 2015; FDA authorised it on 2 April 2025; FDA authorised it on 27 August 2025.

Who is the marketing authorisation holder for Victoza in United States?

NOVO NORDISK INC holds the US marketing authorisation.