[Congressional Bills 117th Congress]
[From the U.S. Government Publishing Office]
[H.R. 7653 Introduced in House (IH)]
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117th CONGRESS
2d Session
H. R. 7653
To amend the Federal Food, Drug, and Cosmetic Act to modernize the
methods of authenticating controlled substances in the pharmaceutical
distribution supply chain, and for other purposes.
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IN THE HOUSE OF REPRESENTATIVES
May 3, 2022
Mr. Mullin (for himself and Mr. O'Halleran) introduced the following
bill; which was referred to the Committee on Energy and Commerce
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A BILL
To amend the Federal Food, Drug, and Cosmetic Act to modernize the
methods of authenticating controlled substances in the pharmaceutical
distribution supply chain, 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 ``Modern Authentication of
Pharmaceuticals Act of 2022''.
SEC. 2. MODERNIZING THE AUTHENTICATION OF CONTROLLED SUBSTANCES IN THE
PHARMACEUTICAL DISTRIBUTION SUPPLY CHAIN.
(a) In General.--Section 582(a)(9) of the Federal Food, Drug, and
Cosmetic Act (21 U.S.C. 360eee-1(a)(9)) is amended--
(1) in subparagraph (A)(ii), by striking ``and'' at the
end;
(2) by redesignating subparagraph (B) as subparagraph (C);
and
(3) by inserting after subparagraph (A) the following:
``(B) a physical chemical identifier shall be
included in or on each dose of a product that is--
``(i) a controlled substance (as defined in
section 102 of the Controlled Substances Act);
``(ii) in solid oral dosage form; and
``(iii) manufactured on or after January 1,
2026; and''.
(b) Conforming Changes.--
(1) Section 581(14) of the Federal Food, Drug, and Cosmetic
Act (21 U.S.C. 360eee(14)) is amended to read as follows:
``(14) Product identifier.--The term `product identifier'
means--
``(A) a standardized graphic that includes, in both
human-readable form and on a machine-readable data
carrier that conforms to the standards developed by a
widely recognized international standards development
organization, the standardized numerical identifier,
lot number, and expiration date of the product; or
``(B) a physical chemical identifier, possessing a
unique physical or chemical substance or combination of
substances, that--
``(i) is in or on a product;
``(ii) is machine-readable; and
``(iii) is intended to authenticate the
product or a dosage form thereof.''.
(2) Section 581(28) of the Federal Food, Drug, and Cosmetic
Act (21 U.S.C. 360eee(28)) is amended to read as follows:
``(28) Verification or verify.--The term `verification' or
`verify' means--
``(A) determining whether the product identifier
affixed to, or imprinted upon, a package or homogeneous
case corresponds to the standardized numerical
identifier or lot number and expiration date assigned
to the product by the manufacturer or the repackager,
as applicable in accordance with section 582; or
``(B) determining whether a product or a dosage
form thereof is authentic using a physical chemical
identifier described in paragraph (14)(B).''.
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