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Suboxone Review: Potential Changes in Availability and Regulations

This act mandates a scientific and medical review of Suboxone (buprenorphine-naloxone), used in addiction treatment. The goal is to assess if current regulations for this medication are still appropriate. This could impact how the drug is accessed and prescribed to patients in the future.
Key points
The Department of Health and Human Services will review current scientific and medical data on Suboxone.
The Attorney General, based on these findings, may change the drug's classification rules, affecting its availability.
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Additional Information
Print number: 118_HR_4053
Sponsor: Rep. Kuster, Ann M. [D-NH-2]
Process start date: 2023-06-13
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Summarized by: gemini-2.5-flash-preview-05-20
Source data: api.congress.gov
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OFFICIAL LEGAL TITLE

Studying Suboxone Act

FREQUENTLY ASKED QUESTIONS

What is the official ID of this bill?

The official print number for this legislation is 118_HR_4053.

Which chamber initiated this legislation?

This legislation was initiated in the House of Representatives.

When did the legislative process begin?

The process officially started on 2023-06-13.

What are the main provisions?

Key points include:

  • The Department of Health and Human Services will review current scientific and medical data on Suboxone.
  • The Attorney General, based on these findings, may change the drug's classification rules, affecting its availability.
What is the specific legal status?

The current status is Expired.

Where can I read the full text of this legislation?

The full official text is available at: View full text

Who is the primary sponsor?

The primary sponsor is Rep. Kuster, Ann M. [D-NH-2].

What is the latest detailed status?

The latest detailed status is: Referred to the Subcommittee on Health.

Is this summary verified?

Yes. This content was analyzed by AI and verified by the Lustra Judge System on 2025-12-25.

CATEGORIES

Health