The attorneys general of Louisiana, Idaho and Missouri filed a lawsuit in October 2025 in a Louisiana federal court, seeking to overturn the U.S. Food and Drug Administration’s 2023 decision to allow telehealth abortion. (The Louisiana lawsuit is one of three currently active lawsuits filed by state attorneys general pushing the FDA to roll back access to mifepristone.)
Now, mifepristone’s manufacturers are moving to join the lawsuit and defend access to medication abortion.
On Feb. 3, Danco Laboratories and GenBioPro—manufacturers of the brand-name and a generic of mifepristone—filed motions to intervene, opposing Louisiana’s request for a preliminary injunction and urging the court to dismiss the lawsuit. The drugmakers argue that mifepristone has a long-established safety record—proven safe beyond any doubt by over 100 peer-reviewed studies and 25 years of real-world use by more than 7.5 million women.
GenBioPro explained its reasons for filing the motion. “We are increasingly concerned by extremists’ complete disregard for the large body of scientific evidence supporting mifepristone’s use and safety,” said GenBioPro CEO Evan Masingill. “We will not stand by while politically motivated efforts put Americans’ access to medication abortion in jeopardy.”
The next hearing in the Louisiana et al. v FDA case is set for Feb. 24, when Judge David Joseph will hear arguments on Louisiana’s preliminary injunction motion to block telehealth abortion and pharmacy dispensing of mifepristone.











