Trump Administration Responds to Lawsuit Seeking Immediate Nationwide Restrictions on Medication Abortion
Department of Justice does not defend Americans’ ability to access medication abortion but seeks to pause the case based on a politically motivated FDA review already underway
NEW ORLEANS —Today, the Trump administration filed a brief on behalf of the Food and Drug Administration (FDA) in a lawsuit that threatens to limit nationwide access to mifepristone, a safe and effective medication used in two-thirds of U.S. abortions and miscarriage care, within the next few months. The Department of Justice (DOJ) argues that the case, Louisiana v. FDA, should not move forward because the FDA has already undertaken a new review of its regulations on mifepristone. At no point in the brief did the DOJ defend the merits of the FDA’s evidence-based decision to allow mifepristone patients to fill their prescription by mail and at pharmacies, the issue at the core of the case. To the contrary, the Trump administration took the unusual step of criticizing the multi-year scientific analysis that led the FDA to lift its in-person dispensing requirement for mifepristone in 2023 — a decision endorsed by every leading medical association — as reflecting a “lack of adequate consideration.”
Mifepristone’s excellent safety record, including when prescribed through telemedicine, has been confirmed by more than a hundred peer-reviewed studies and leading medical authorities like the American Medical Association and the American College of Obstetricians and Gynecologists. By contrast, the Trump administration’s announcement last spring that it would undertake a new review of its mifepristone regulations was based on a debunked, self-published paper from a Project 2025 sponsor that purposefully distorts the safety record of medication abortion and has been denounced by more than 260 expert researchers for its severe scientific flaws.
The DOJ’s brief in Louisiana indicates that the Trump administration expects to complete its mifepristone review in less than a year.
“Don’t be fooled: the Trump administration isn’t defending medication abortion — it’s just defending its own authority to restrict access to mifepristone if, when, and how it sees fit,” said Julia Kaye, senior staff attorney with the American Civil Liberties Union’s Reproductive Freedom Project. “The state politicians attacking mifepristone in court and the Trump administration officials ordering a new FDA review are two sides of the same coin — and both are wrong on the law, the science, and public opinion. Any new federal restrictions on medication abortion would not only be medically and legally unjustified but deeply unpopular among the overwhelming majority of Americans.”
Louisiana’s lawsuit could severely hinder medication abortion access across the country as soon as late February. Recent data show that by June 2025, more than 1 in 4 abortions in the U.S. were provided via telemedicine using mifepristone. This method of care could be halted immediately if the federal district court in Louisiana grants the state’s request to impose sweeping nationwide restrictions. A ruling could come any time after a hearing scheduled for Feb. 24.
Louisiana is seeking to prevent patients from being able to fill their mifepristone prescription by mail or at a local pharmacy. Instead, patients all across the country, including in states where abortion care is legally protected, would be required to pick up the pill in person at a hospital, clinic, or medical office — even when they have already received care through telemedicine and there is no medical reason for the trip. Accessing abortion via telemedicine is especially important for people who live on low incomes; who struggle to secure transportation, childcare, or time off work; who live in rural areas; and who are experiencing domestic violence. Any restrictions on mifepristone would also affect patients using the medication for miscarriage management.
Louisiana v. FDA is one of three pending federal lawsuits brought by anti-abortion state politicians trying to end the use of telemedicine for mifepristone. The other two suits — Missouri v. FDA and Florida v. FDA — seek to impose other nationwide restrictions on mifepristone as well, and Florida seeks to ban the medication altogether by undoing FDA’s original approval from 25 years ago.