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HR 9790
Introduced Re-checks Congress.gov for new actions and updates the bill's status, and fills in any sponsors, committees, or related bills that are missing. It does not re-pull sponsors/cosponsors/committees/related — those rarely change — and it skips all work if nothing has changed upstream, so it's cheap to click.

Modernizing Opioid Treatment Access Act 2.0 of 2026

To expand access to methadone through alternative care models using pharmacies.

Introduced Jul 20, 2026

Latest action (Jul 20, 2026) Referred to the Committee on Energy and Commerce, and in addition to the Committee on the Judiciary, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned.

Summary

  • Allows qualified addiction medicine physicians and addiction psychiatrists to be registered to prescribe methadone for opioid use disorder to be dispensed through pharmacies, in addition to traditional opioid treatment programs.
  • Permits methadone to be prescribed through electronic prescribing only and dispensed in liquid or dispersible tablet formulations to individuals for supervised or unsupervised use.
  • Allows methadone treatment to be provided through telemedicine and requires practitioners to obtain informed consent from patients that includes disclosure of differences in confidentiality protections between pharmacy and treatment program dispensing.
  • Eliminates the requirement for pharmacies to obtain separate registration in order to dispense methadone prescribed under this new process.
  • Allows states to opt out of the program by requesting that the Attorney General cease registrations and revoke existing registrations of practitioners in that state.
  • Requires the Drug Enforcement Administration to submit annual reports to Congress on the number of registered practitioners by state, pharmacy orders, and any violations related to the new methadone prescribing authority.

AI-generated plain-language summary of the bill text — neutral, and may be imperfect. See the full text below for the exact wording.

Sponsor (1)

Money behind the sponsor

Top reported contributors to Donald Norcross’s campaign committee (2024 cycle) — who funds the bill’s sponsor, not a claim about this bill. Data from FEC.

  • WESTERN EXTRUSIONS $26,000
  • HOLTEC INTERNATIONAL $14,150
  • COOPER UNIVERSITY HEALTH CARE $13,200
  • CURRENT MASTER ELECTRIC $13,200
  • BACH ASSOCIATES, PC $13,200

Organizations whose employees gave the most — itemized individual contributions grouped by the donor’s reported employer (FEC Schedule A). Full finance for Donald Norcross → · Outside spending →

Actions (2)

  1. Jul 20, 2026 Referred to the Committee on Energy and Commerce, and in addition to the Committee on the Judiciary, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned. · house
  2. Jul 20, 2026 Introduced in House

Similar bills (6)

Bills with similar text or summary — includes reintroductions across Congresses. Ranked by semantic similarity of the bill text (computed locally); a neutral discovery aid, not a claim the bills are duplicates.

Full text

IN THE HOUSE OF REPRESENTATIVES

July 20, 2026

Mr. Norcross (for himself, Mr. Lawler, and Mr. Tonko) introduced the following bill; which was referred to the Committee on Energy and Commerce, and in addition to the Committee on the Judiciary, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned

A BILL

To expand access to methadone through alternative care models using pharmacies.

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 “Modernizing Opioid Treatment Access Act 2.0 of 2026”.

SEC. 2. EXPANSION OF METHADONE FOR OPIOID USE DISORDER THROUGH PRESCRIBING AND PHARMACIES.

Section 303(h) of the Controlled Substances Act (21 U.S.C. 823(h)) is amended—

(1) in paragraph (2)—

(A) by striking “(A)” and inserting “(i)”; and

(B) by striking “(B)” and inserting “(ii)”;

(2) by redesignating paragraphs (1), (2), and (3) as subparagraphs (A), (B), and (C), respectively;

(3) by striking “(h) Practitioners” and inserting

“(h)(1) Practitioners”; and

(4) by adding at the end the following:

“(2)(A) The requirements of paragraph (1) applicable to methadone medication for opioid use disorder are waived, and the Attorney General, in consultation with the Secretary, shall separately register practitioners described in subparagraph (B) of this paragraph to prescribe methadone for opioid use disorder to be dispensed through a pharmacy to individuals for their own supervised or unsupervised use.

“(B) Practitioners described in this subparagraph are persons who—

“(i) are licensed, registered, or otherwise permitted, by the United States or the jurisdiction in which they practice, to prescribe controlled substances in the course of professional practice; and

“(ii) are—

“(I) addiction medicine physicians or addiction psychiatrists who hold a subspecialty board certification in addiction medicine from the American Board of Preventive Medicine, a board certification in addiction medicine from the American Board of Addiction Medicine, a subspecialty board certification in addiction psychiatry from the American Board of Psychiatry and Neurology, or a subspecialty board certification in addiction medicine from the American Osteopathic Association; or

“(II) otherwise determined by the Secretary, under standards established by the Secretary, to be qualified to prescribe methadone for opioid use disorder.

“(C) The prescribing of methadone pursuant to subparagraph (A) shall be—

“(i) exclusively by electronic prescribing and dispensed to the individual treated pursuant to subparagraph (A);

“(ii) in compliance with applicable Federal and State law respecting the quantities of methadone for opioid use disorder that may be dispensed to individuals pursuant to subparagraph

(A); and

“(iii) for a liquid or dispersible tablet formulation.

“(D) The dispensing of methadone to an individual pursuant to subparagraph (A) shall be in addition to the other care that the individual continues to have access to through an opioid use disorder treatment program.

“(E) Practitioners registered pursuant to subparagraph (A) shall—

“(i) ensure and document, with respect to each individual treated pursuant to subparagraph (A), informed consent to treatment; and

“(ii) include in such informed consent, specific informed consent regarding differences in confidentiality protections applicable when dispensing through an opioid treatment program versus dispensing through a pharmacy pursuant to subparagraph

(A).

“(F) At the request of a State, the Attorney General shall—

“(i) cease registering persons in the State pursuant to subparagraph (A);

“(ii) revoke any such registration in effect for a person in the State pursuant to section 304; and

“(iii) deny any pending application for such registration from a practitioner in the State pursuant to section 304.

“(G) Maintenance treatment or detoxification treatment provided pursuant to subparagraph (A) may be provided through the practice of telemedicine.

“(H) A pharmacy shall not be required to obtain a separate registration to dispense methadone medication for opioid use disorder to an individual who has been prescribed that medication by a practitioner registered pursuant to subparagraph (A).

“(3) Not later than 180 days after the date of enactment of this paragraph, and annually thereafter, the Administrator of the Drug Enforcement Administration shall submit to Congress a report that includes, for the reporting period—

“(A) the number of practitioners registered pursuant to paragraph (2)(A) in each State;

“(B) a list of States for which the Attorney General received a request pursuant to paragraph (2)(F);

“(C) the number of revocations or suspensions of registration issued pursuant to section 304, based on violations related to the prescribing of methadone for opioid use disorder by practitioners who are registered pursuant to paragraph (2)(A); and

“(D) the number of pharmacies that ordered methadone in liquid or dispersible tablet formulations.”.

SEC. 3. EFFECTIVE DATE.

This Act and the amendments made by this Act shall take effect on the date that is 180 days after the date of enactment of this Act. <all>

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