🇺🇸 Anastrazole (Arimidex) in United States

FDA authorised Anastrazole (Arimidex) on 5 December 2008

Marketing authorisation

FDA — authorised 5 December 2008

  • Application: NDA022214
  • Marketing authorisation holder: ASTRAZENECA
  • Local brand name: ARIMIDEX
  • Indication: TABLET — ORAL
  • Status: approved

Read official source →

Other Oncology approved in United States

Frequently asked questions

Is Anastrazole (Arimidex) approved in United States?

Yes. FDA authorised it on 5 December 2008.

Who is the marketing authorisation holder for Anastrazole (Arimidex) in United States?

ASTRAZENECA holds the US marketing authorisation.