A coalition of pro-life advocates led by Live Action President Lila Rose on Friday urged Health and Human Services Secretary Robert F. Kennedy Jr. and FDA Commissioner Marty Makary to reverse the recent approval of an abortion drug. 
Over two dozen pro-life advocates petitioned the FDA following the agency&#8217;s Tuesday approval of Evita Solutions’ generic version of mifepristone, the drug used in over 60% of all abortions. The signatories say that instead of approving new life-ending drugs, the FDA should completely remove mifepristone from the market. 
“We urge you, in the strongest possible terms, to reverse this dangerous approval immediately,&#8221; the coalition wrote, according to a <a href="https://dw-wp-production.imgix.net/2025/10/FDA-Coalition-Letter_-Abortion-Pill-10.3.2025-1.pdf">copy of the letter</a> obtained by The Daily Wire. &#8220;Rather than expanding the license for these drugs, the FDA should acknowledge the clear evidence of harm and withdraw mifepristone from the market.&#8221;
“Every abortion is a violation of human rights, and every life lost is an irreplaceable son or daughter. The federal government must stop enabling this violence under the false banner of ‘healthcare,’” they added. 
Signers of the letter included Ethics and Public Policy Center President Ryan Anderson, Students for Life President Kristan Hawkins, and Concerned Women for America CEO Penny Nance.
On Friday, White House Press Secretary Karoline Leavitt said that the administration did not endorse the drug, but was required by law to approve Evita’s application because it was a generic offering of a drug already offered by two other pharmaceutical companies. 
The letter to Kennedy also laid out the brutal process that takes place after a mother takes a chemical abortion pill. 
“A chemical abortion consists of a two-step process. First, a pregnant mother will take mifepristone to starve her preborn child to death. Next, she will take misoprostol to induce labor contractions and deliver the baby&#8217;s dead body. At this stage in the first trimester, children developing in the womb already have a detectable heartbeat and brainwaves, and are beginning to move their arms and legs,” the coalition wrote. 
The coalition said that the approval contradicted a recent commitment from Kennedy to study the dangers of mifepristone. 
“Yet rather than pausing to examine the mounting evidence showing the harmful effects of mifepristone, the FDA has chosen to expand access to a drug that has already killed millions of preborn children and harmed countless women, undermining the very commitment that the Secretary publicly made to protect patients,” they wrote. 
Chemical abortions account for about two-thirds of all abortions in the United States and have ended the lives of at least 7.5 million unborn babies. At the same time, the mothers who take the pills often experience additional medical complications like hemorrhaging and sepsis. Studies showing the dangers of the drug have been manipulated to hide the harm, the coalition said. 
The decision has already triggered outrage from many Republican lawmakers. Senator Josh Hawley (R-MO) said he had completely lost faith in the FDA over the move, while over a dozen Republican representatives <a href="https://www.dailywire.com/news/republicans-demand-rfk-fire-rogue-actors-at-fda-who-approved-abortion-drug?author=Leif+Le+Mahieu&amp;category=News&amp;elementPosition=1&amp;row=0&amp;rowType=Vertical+List&amp;title=Republicans+Demand+RFK+Fire+%E2%80%98Rogue+Actors%E2%80%99+At+FDA+Who+Approved+Abortion+Drug">sent a letter</a> on Friday telling Kennedy to fire the “rogue actors” at the agency who approved the lethal drug. 

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‘Every Abortion Is A Violation Of Human Rights’: Pro-Life Advocates Demand FDA Yank Abortion Drug

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‘Every Abortion Is A Violation Of Human Rights’: Pro-Life Advocates Demand FDA Yank Abortion Drug