S.Amdt. 1072Senate116th Congress (2019-2021)2nd degree

S.Amdt. 1072

Submitted October 24, 2019

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Senate amendment submitted

October 24, 2019

Text

Submitted

SA 1072. Mr. MARKEY (for himself, Mr. Braun, and Mr. Manchin)
submitted an amendment intended to be proposed to amendment SA 948
proposed by Mr. Shelby to the bill H.R. 3055, making appropriations for
the Departments of Commerce and Justice, Science, and Related Agencies
for the fiscal year ending September 30, 2020, and for other purposes;
which was ordered to lie on the table; as follows:

At the appropriate place in division B, insert the
following:

SEC. __. OPIOID LABELING REQUIREMENTS.

(a) In General.--Section 305(c) of the Controlled
Substances Act (21 U.S.C. 825(c)) is amended--
(1) by inserting ``(1)'' before ``The Secretary''; and
(2) by adding at the end the following:
``(2) The label of any container or package containing an
opioid or opiate listed in schedule II, III, IV, or V shall,
when dispensed (other than administered) to or for a patient,
contain a clear, concise warning, in a manner specified by
the Secretary by regulation, that the opioids or opiates
dispensed can cause dependence, addiction, and overdose.''.
(b) Regulations.--
(1) Regulations.--The Secretary of Health and Human
Services shall prescribe regulations under section 503(b) of
the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 353(b))
to implement the amendment made by subsection (a) and such
regulations shall be effective not later than 2 years after
the date of enactment of this Act.
(2) Interim rules.--The Secretary of Health and Human
Services may issue the regulations required under paragraph
(1) by interim rule to the extent necessary to comply with
the timing requirement in paragraph (1).
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