United States · Bill · HR
H.R. 4053 (118th)
Studying Suboxone Act
Introduced
13 June 2023
Last action
—
Status
Referred to the Subcommittee on Health.
Sponsors
—
Subjects
Discovery layer
Source updated
27 May 2025
Summary
Studying Suboxone Act This bill requires the Department of Health and Human Services (HHS) and the Drug Enforcement Administration (DEA) to reevaluate the scheduling of buprenorphine-naloxone combination products (e.g., suboxone) under the Controlled Substances Act. These products are used to treat opioid addictions and are currently schedule III controlled substances. (A schedule III controlled substance is a drug, substance, or chemical that has less potential for abuse than a schedule I or II substance; that has a currently accepted medical use; and that has low or moderate risk of dependence if abused.) Specifically, the bill requires HHS to review scientific and medical evaluations relating to these products and update its scheduling recommendations accordingly. The DEA must review the recommendations of HHS and make appropriate scheduling changes.
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Documents
3 official files
Introduced in House (text)
Introduced in House (text)
Introduced in House · EN · 13 June 2023
Introduced in House (PDF)
Introduced in House · EN · 13 June 2023
Introduced in House
summary · EN · 13 June 2023
Sponsors
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Related records
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Sources
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- Official source: https://www.congress.gov/bill/118th-congress/house-bill/4053
- Open data entity: https://api.congress.gov/v3/bill/118/hr/4053