🇺🇸 Placebo for "Deficiency of Qi and Yang" in United States

FDA authorised Placebo for "Deficiency of Qi and Yang" on 17 October 1974

Marketing authorisations

FDA — authorised 17 October 1974

  • Application: ANDA080767
  • Marketing authorisation holder: IMPAX LABS
  • Status: supplemented

FDA — authorised 28 August 1981

  • Application: ANDA086173
  • Marketing authorisation holder: FOSUN PHARMA
  • Status: supplemented

FDA — authorised 17 September 2010

  • Application: ANDA079025
  • Marketing authorisation holder: CHARTWELL RX
  • Status: approved

FDA — authorised 21 December 2011

  • Application: ANDA090653
  • Marketing authorisation holder: HOSPIRA INC
  • Status: approved

FDA — authorised 26 June 2012

  • Application: ANDA090979
  • Marketing authorisation holder: PADAGIS ISRAEL
  • Status: approved

Frequently asked questions

Is Placebo for "Deficiency of Qi and Yang" approved in United States?

Yes. FDA authorised it on 17 October 1974; FDA authorised it on 28 August 1981; FDA authorised it on 17 September 2010.

Who is the marketing authorisation holder for Placebo for "Deficiency of Qi and Yang" in United States?

IMPAX LABS holds the US marketing authorisation.