FDA to Review Data on Long-Term Use of Myfembree for Uterine Fibroids
The Food and Drug Administration (FDA) has accepted for review the supplemental New Drug Application (sNDA) for Myfembree® (relugolix 40mg, estradiol 1mg, and norethindrone acetate 0.5mg). The sNDA proposes to update the prescribing information to…