Company Seeks Federal License to Make Ibogaine and Psilocybin
Published Date: 10/19/2026
Notice
Summary
Groff Health Inc wants to become a big-time maker of some powerful controlled substances like Ibogaine and Psilocybin. This means they’ll produce these drugs in large amounts for their own use and to sell to customers. If you have thoughts or objections, you’ve got until December 18, 2026, to speak up online or ask for a hearing.
No Economic Impacts Identified for this Document
Personalized for You
How does this regulation affect your finances?
Personalize government policy and PRIA will tell you what this federal register document means for your household, plus every other regulation we track. PRIA reads each provision against your financial profile to show you exactly what matters to your wallet.
Key Dates
Department and Agencies
Related Federal Register Documents
2026-11526, Implementation of the Substance Use-Disorder Prevention That Promotes Opioid Recovery and Treatment for Patients and Communities Act of 2018: Dispensing and Administering Controlled Substances for Medication-Assisted Treatment
Starting July 9, 2026, new rules make it easier for doctors and pharmacies to provide medicine that helps people recover from opioid addiction. These changes affect healthcare providers by expanding who can give medication-assisted treatment and how pharmacies can deliver these medicines. The goal? Faster, safer access to treatment with clear rules that save time and support recovery.
2026-10128, Revision of Applications for Manufacturing and Procurement Quotas
The DEA wants to update how companies apply for permission to make and buy certain controlled drugs and chemicals. These changes will make the rules clearer, help prevent drug shortages, and ensure enough supply for medical and scientific needs. If you’re a manufacturer or involved in this process, get ready to follow new steps and share your thoughts by July 20, 2026.
2025-05007, Expansion of Buprenorphine Treatment via Telemedicine Encounter and Continuity of Care via Telemedicine for Veterans Affairs Patients
Starting December 31, 2025, veterans can get buprenorphine treatment and follow-up care through telemedicine, making it easier to access help for opioid use disorder without leaving home. This change affects veterans using VA health services and aims to improve treatment access while the government reviews feedback and policies. No new costs are mentioned, but the delay gives agencies time to ensure the rules work well.
2025-02793, Expansion of Buprenorphine Treatment via Telemedicine Encounter and Continuity of Care via Telemedicine for Veterans Affairs Patients
The government is giving veterans easier access to buprenorphine treatment through telemedicine, letting them get care remotely. This change affects veterans using VA health services and aims to make treatment smoother and more convenient. The new rules were supposed to start February 18, 2025, but now they’ll kick in on March 21, 2025, while the government gathers public feedback.
2026-21413, Jefferson Burroughs, M.D.; Decision and Order
Dr. Jefferson Burroughs from Ohio lost his DEA registration to handle controlled substances because he no longer has the legal authority to prescribe them in his state. He didn’t ask for a hearing to challenge this, so the DEA officially revoked his registration as of July 31, 2026. This means Dr. Burroughs can’t legally prescribe or manage controlled drugs anymore, affecting his medical practice and patients.
2026-21414, Jan Pijanowski, M.D.; Decision and Order
Dr. Jan Pijanowski from Ohio lost his DEA registration because his medical license expired and he didn’t respond to the DEA’s notice. This means he can no longer prescribe or handle controlled substances, effective immediately. If you’re a patient or pharmacy, this change is official as of October 2026 and affects any prescriptions tied to him.
Previous / Next Documents
Previous: 2026-21367, Importer of Controlled Substances Application: Groff NA Hemplex LLC
Groff NA Hemplex LLC wants to become an official importer of certain controlled substances like marijuana and its extracts. People and companies involved with these substances can share their thoughts or ask for a hearing by November 18, 2026. This move could shake up how these substances enter the U.S., so keep an eye on the deadlines and get ready to comment if you’re affected!
Next: 2026-21369, Bulk Manufacturer of Controlled Substances Application: Janssen Pharmaceuticals, Inc.
Janssen Pharmaceuticals wants to officially make a big batch of methylphenidate, a controlled drug, at their Georgia site. People who already make or use this drug can share their thoughts or ask for a hearing by December 18, 2026. This move could affect how the drug is produced and sold, but no extra activities are allowed beyond manufacturing for sale.