Federal
Opioid Prescription Verification Act of 2021
Source: Congress.gov ·
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IIB
117TH CONGRESS
1ST SESSION H. R. 2355
IN THE SENATE OF THE UNITED STATES
DECEMBER 9, 2021
Received; read twice and referred to the Committee on Health, Education,
Labor, and Pensions
AN ACT
To facilitate responsible, informed dispensing of controlled
substances and other prescribed medications, and for
other purposes.
Be it enacted by the Senate and House of Representa-
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tives of the United States of America in Congress assembled,
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HR 2355 RFS
SECTION 1. SHORT TITLE.
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This Act may be cited as the ‘‘Opioid Prescription
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Verification Act of 2021’’.
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SEC. 2. MATERIALS FOR TRAINING PHARMACISTS ON CER-
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TAIN
CIRCUMSTANCES
UNDER
WHICH
A
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PHARMACIST MAY DECLINE TO FILL A PRE-
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SCRIPTION.
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(a) UPDATES TO MATERIALS.—Section 3212(a) of
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the SUPPORT for Patients and Communities Act (21
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U.S.C. 829 note) is amended by striking ‘‘Not later than
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1 year after the date of enactment of this Act, the Sec-
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retary of Health and Human Services, in consultation with
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the Administrator of the Drug Enforcement Administra-
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tion, Commissioner of Food and Drugs, Director of the
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Centers for Disease Control and Prevention, and Assistant
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Secretary for Mental Health and Substance Use, shall de-
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velop and disseminate’’ and inserting ‘‘The Secretary of
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Health and Human Services, in consultation with the Ad-
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ministrator of the Drug Enforcement Administration,
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Commissioner of Food and Drugs, Director of the Centers
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for Disease Control and Prevention, and Assistant Sec-
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retary for Mental Health and Substance Use, shall develop
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and disseminate not later than 1 year after the date of
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enactment of this Act, and update periodically thereafter’’.
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HR 2355 RFS
(b) MATERIALS INCLUDED.—Section 3212(b) of the
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SUPPORT for Patients and Communities Act (21 U.S.C.
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829 note) is amended—
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(1) by redesignating paragraphs (1) and (2) as
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paragraphs (2) and (3), respectively; and
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(2) by inserting before paragraph (2), as so re-
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designated, the following new paragraph:
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‘‘(1) pharmacists on how to verify the identity
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of the patient;’’.
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(c)
MATERIALS
FOR
TRAINING
ON
PATIENT
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VERIFICATION .—Section 3212 of the SUPPORT for Pa-
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tients and Communities Act (21 U.S.C. 829 note) is
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amended by adding at the end the following new sub-
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section:
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‘‘(d) MATERIALS FOR TRAINING ON VERIFICATION
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OF IDENTITY.—Not later than 1 year after the date of
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enactment of this subsection, the Secretary of Health and
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Human Services, after seeking stakeholder input in ac-
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cordance with subsection (c), shall—
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‘‘(1) update the materials developed under sub-
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section (a) to include information for pharmacists on
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how to verify the identity the patient; and
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‘‘(2) disseminate, as appropriate, the updated
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materials.’’.
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SEC. 3. INCENTIVIZING STATES TO FACILITATE RESPON-
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SIBLE,
INFORMED
DISPENSING
OF
CON-
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TROLLED SUBSTANCES.
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(a) IN GENERAL.—Section 392A of the Public
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Health Service Act (42 U.S.C. 280b–1) is amended—
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(1) by redesignating subsections (c) and (d) as
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subsections (d) and (e), respectively; and
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(2) by inserting after subsection (b) the fol-
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lowing new subsection:
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‘‘(c) PREFERENCE.—In determining the amounts of
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grants awarded to States under subsections (a) and (b),
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the Director of the Centers for Disease Control and Pre-
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vention may give preference to States in accordance with
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such criteria as the Director may specify and may choose
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to give preference to States that—
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‘‘(1) maintain a prescription drug monitoring
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program;
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‘‘(2) require prescribers of controlled substances
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in schedule II, III, or IV to issue such prescriptions
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electronically, and make such requirement subject to
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exceptions in the cases listed in section 1860D–
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4(e)(7)(B) of the Social Security Act; and
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‘‘(3) require dispensers of such controlled sub-
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stances to enter certain information about the pur-
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chase of such controlled substances into the respec-
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HR 2355 RFS
tive State’s prescription drug monitoring program,
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including—
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‘‘(A) the National Drug Code or, in the
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case of compounded medications, compound
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identifier;
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‘‘(B) the quantity dispensed;
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‘‘(C) the patient identifier; and
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‘‘(D) the date filled.’’.
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(b) DEFINITIONS.—Subsection (d) of section 392A of
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the Public Health Service Act (42 U.S.C. 280b–1), as re-
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designated by subsection (a)(1), is amended to read as fol-
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lows:
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‘‘(d) DEFINITIONS.—In this section:
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‘‘(1) CONTROLLED
SUBSTANCE.—The term
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‘controlled substance’ has the meaning given that
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term in section 102 of the Controlled Substances
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Act.
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‘‘(2) DISPENSER.—The term ‘dispenser’ means
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a physician, pharmacist, or other person that dis-
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penses a controlled substance to an ultimate user.
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‘‘(3) INDIAN TRIBE.—The term ‘Indian tribe’
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has the meaning given that term in section 4 of the
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Indian Self-Determination and Education Assistance
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Act.’’.
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Passed the House of Representatives December 8,
2021.
Attest:
CHERYL L. JOHNSON,
Clerk.
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