Supreme Court is asked to reject limits on a drug used in the most common method of abortion

In an appeal filed Friday, Sept. 8, 2023, Danco Laboratories, the manufacturer of mifepristone, argued that federal judges should not second-guess the Food and Drug Administration’s approval of the drug or the conditions under which it is dispensed. The Biden administration also was expected to file an appeal.

Boxes of the drug mifepristone sit on a shelf at the West Alabama Women’s Center in Tuscaloosa, Ala., on March 16, 2022. In an appeal filed Friday, Sept. 8, 2023, Danco Laboratories, the manufacturer of mifepristone, argued that federal judges should not second-guess the Food and Drug Administration’s approval of the drug or the conditions under which it is dispensed. The Biden administration also was expected to file an appeal.

Light illuminates part of the Supreme Court building on Capitol Hill in Washington, Nov. 16, 2022. In an appeal filed Friday, Sept. 8, 2023, Danco Laboratories, the manufacturer of mifepristone, argued that federal judges should not second-guess the Food and Drug Administration’s approval of the drug or the conditions under which it is dispensed. The Biden administration also was expected to file an appeal.

A patient prepares to take the first of two combination pills, mifepristone, for a medication abortion during a visit to a clinic in Kansas City, Kan., Oct. 12, 2022. In an appeal filed Friday, Sept. 8, 2023, Danco Laboratories, the manufacturer of mifepristone, argued that federal judges should not second-guess the Food and Drug Administration’s approval of the drug or the conditions under which it is dispensed. The Biden administration also was expected to file an appeal.

A patient prepares to take the first of two combination pills, mifepristone, for a medication abortion during a visit to a clinic in Kansas City, Kan., Oct. 12, 2022. In an appeal filed Friday, Sept. 8, 2023, Danco Laboratories, the manufacturer of mifepristone, argued that federal judges should not second-guess the Food and Drug Administration’s approval of the drug or the conditions under which it is dispensed. The Biden administration also was expected to file an appeal.

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