FDA — authorised 17 October 1974
- Application: ANDA080767
- Marketing authorisation holder: IMPAX LABS
- Status: supplemented
FDA authorised Placebo for "Deficiency of Qi and Yin" on 17 October 1974
Yes. FDA authorised it on 17 October 1974; FDA authorised it on 28 August 1981; FDA authorised it on 17 September 2010.
IMPAX LABS holds the US marketing authorisation.