Shown verbatim: the complete text as captured from the official PDF posted by the Tennessee General Assembly, fetched 2026-09-25. Page and line markers are part of the official record; nothing is edited or removed. This is the chaptered version. The official bill page.
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~tate of \lrennessee
PUBLIC CHAPTER NO. 1008
HOUSE BILL NO. 2136
By Representatives Terry, Davis, Russell, Howell
Substituted for: Senate Bill No. 2556
By Senators Reeves, Stevens
AN ACT to amend Tennessee Code Annotated, Title 39; Title 53; Title 63 and Title 68,
relative to medications approved by the federal food and drug administration.
BE IT ENACTED BY THE GENERAL ASSEMBLY OF THE STATE OF TENNESSEE:
SECTION 1. Tennessee Code Annotated, Section 39-17-403(d), is amended by
designating the existing language as subdivision (d)(1) and adding the following as a new
subdivision:
(2) If no objection is filed under subdivision (d)(1) for a substance that is
approved by the United States food and drug administration and designated or
scheduled under federal law by a final order published in the Federal Register, then the
substance is considered to be in the same schedule as such substance is designated or
scheduled under the federal schedule of controlled substances after the expiration of
thirty (30) days from the date of publication of the final order. Any such designation or
scheduling pursuant to this subdivision (d)(2) is effective immediately after the expiration
of thirty (30) days from the date of publication of the final order and is not contingent on
the annual revision and republishing of schedules pursuant to subsection (g).
SECTION 2. Tennessee Code Annotated, Title 63, Chapter 1, Part 1, is amended by
adding the following as a new section:
(a) Notwithstanding a law to the contrary, a healthcare prescriber licensed under
this title who is authorized to prescribe controlled substances may prescribe a drug
product that has been scheduled pursuant to § 39-17-403(d)(2) immediately upon the
effective date of such scheduling if:
(1) The drug product is approved by the United States food and drug
administration;
(2) The drug product is in a schedule other than Schedule I by operation
of§ 39-17-403(d);
(3) Prescribing the drug product is within the healthcare prescriber's
lawful scope of practice; and
(4) The drug product is not otherwise prohibited by state or federal law.
SECTION 3. This act takes effect upon becoming a law, the public welfare requiring it.
HOUSE BILL NO. 2136
PASSED: April 21, 2026
CAMERO7""SEXTON,SPEAKER
HOUSE OF REPRESENTATIVES
~
RANDY MCNALl
SPEAKER OF THE SENAT
Jg-tt. •1 APPROVED this
day of vY'.'r, 2026
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