[Congressional Bills 117th Congress]
[From the U.S. Government Publishing Office]
[H.R. 8976 Introduced in House (IH)]
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117th CONGRESS
2d Session
H. R. 8976
To preempt State restrictions on dispensing mifepristone or
misoprostol, and for other purposes.
_______________________________________________________________________
IN THE HOUSE OF REPRESENTATIVES
September 22, 2022
Mr. Ryan of New York introduced the following bill; which was referred
to the Committee on Energy and Commerce
_______________________________________________________________________
A BILL
To preempt State restrictions on dispensing mifepristone or
misoprostol, and for other purposes.
Be it enacted by the Senate and House of Representatives of the
United States of America in Congress assembled,
SECTION 1. SHORT TITLE.
This Act may be cited as the ``Protecting Reproductive Freedom
Act''.
SEC. 2. PREEMPTION OF STATE RESTRICTIONS ON DISPENSING MIFEPRISTONE AND
MISOPROSTOL.
No State may establish, implement, or enforce--
(1) any prohibition or restriction on shipping or sending
mifepristone or misoprostol across State lines;
(2) any requirement that mifepristone or misoprostol be
dispensed by a health care practitioner in person; or
(3) any prohibition or restriction on prescribing or
dispensing mifepristone or misoprostol by means of telehealth.
SEC. 3. REPORT.
Not later than 30 days after the date of enactment of this Act, the
Secretary of Health and Human Services, acting through the Commissioner
of Food and Drugs, shall submit a report to the Congress on ways to
expand access to abortion medication.
SEC. 4. DEFINITIONS.
In this Act:
(1) The term ``mifepristone'' means mifepristone that is--
(A) approved under subsection (c) or (j) of section
505 of the Federal Food, Drug, and Cosmetic Act (21
U.S.C. 355);
(B) indicated for medical abortion; and
(C) subject to a risk evaluation and mitigation
strategy under section 505-1 of the Federal Food, Drug,
and Cosmetic Act (21 U.S.C. 355-1).
(2) The term ``misoprostol'' means misoprostol that is--
(A) approved under subsection (c) or (j) of section
505 of the Federal Food, Drug, and Cosmetic Act (21
U.S.C. 355);
(B) indicated for medical abortion; and
(C) subject to a risk evaluation and mitigation
strategy under section 505-1 of the Federal Food, Drug,
and Cosmetic Act (21 U.S.C. 355-1).
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