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South Dakota reschedules FDA-approved crystalline polymorph psilocybin to Schedule IV

Original title: reschedule the pharmaceutical composition of crystalline polymorph psilocybin in a drug product approved by the Food and Drug Administration as a Schedule IV controlled substance.

Last action · March 10, 2026: Signed by the GovernorSponsors: Tom Pischke and 12 others

Introduced
Committee
Floor Vote
Passed
Law

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What This Bill Does

South Dakota reclassifies the pharmaceutical composition of psilocybin in an FDA-approved drug product from Schedule I to Schedule IV, easing state restrictions for medical use.

Why it matters

Alters the legal availability and prescription framework for specific FDA-approved psilocybin-based pharmaceutical treatments within the state.

Who It Affects

Groups the bill's text affects, as described in the record. Being affected is not a position for or against it.

Directly affected

Medical patients

Patients may gain legal access to specific FDA-approved psilocybin pharmaceutical treatments under Schedule IV regulations.

Directly affected

Healthcare providers

Providers are subject to updated prescribing and handling rules corresponding to Schedule IV controlled substances.

Key Facts

You don't have to trust us. Each fact below is taken straight from the official document - click any one to see the exact passage, highlighted in the original.

Frequently Asked Questions

Does this bill legalize all forms of psilocybin in South Dakota?
No. Only the specific pharmaceutical composition of psilocybin contained in an FDA-approved drug product is rescheduled to Schedule IV. All other forms of psilocybin remain strictly controlled under Schedule I.
What schedule is crystalline polymorph psilocybin moved to?
It is moved from Schedule I to Schedule IV under South Dakota controlled substances law.

What else do you want to know?

News Coverage

No news coverage found yet. Articles are indexed twice daily.

Where This Stands

Current status: Signed into law.

Procedural history

14 actions
  1. Mar 10, 2026HouseEnrolled
    Signed by the Governor
  2. Mar 5, 2026HouseEnrolled
    Delivered to the Governor
  3. Mar 4, 2026Senate
    Signed by the President
  4. Mar 3, 2026House
    Signed by the Speaker
  5. Mar 2, 2026SenateFloor
    Do Pass
  6. Feb 26, 2026Senate
    Remove from Consent Calendar
Show 8 earlier actions
  1. Feb 25, 2026Senate
    Certified uncontested, placed on consent
  2. Feb 25, 2026SenateCommittee
    Do Pass
  3. Feb 25, 2026Senate
    Scheduled for hearing
  4. Feb 10, 2026SenateIntroduced
    First read in Senate and referred to
  5. Feb 9, 2026HouseFloor
    Do Pass
  6. Feb 5, 2026HouseCommittee
    Do Pass
  7. Feb 5, 2026House
    Scheduled for hearing
  8. Jan 21, 2026HouseIntroduced
    First read in House and referred to

Version history

Only one version on file - nothing to compare yet. As later stages (committee substitute, engrossed, enrolled) are captured, the redline appears here.

View official text →

Voting Record

Motion succeededHouse2/9/2026South Dakota LegislatureOfficial roll call ↗

Do Pass

Total

70

Yes
58
No
7
Present
0
Not voting
0
Abstain
0
Other positions
5

Lobbying Activity

No state lobbying filings in our records match this bill. Federal lobbying reports (LDA) cover Congress, so they are not listed on state bills.

Full breakdown

Who this bill affects and the strongest case for and against it, written only from the bill’s own text.

Sponsors

Connected Entities

Food and Drug Administration, Native American
OrganizationFood and Drug Administration“Federal agency approving drug products”Map →
OrganizationNative American“Mentioned in sacramental peyote exceptions”Map →

Sources

Open source document

sdlegislature.gov

Analysis Score

0–100
  • Significance60
    How much this matters to a regular citizen
  • Controversy40
    Intensity of disagreement among stakeholders
  • Entertainment10
    Compellingness for a non-policy-wonk reader
  • Buzz35
    Current news / social attention level

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