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UN Controls Three Synthetic Drugs, Reviews Coca Leaf

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Summary

The United Nations Commission on Narcotic Drugs (CND) placed three harmful synthetic substances under international control at its 69th session held March 9-13, 2026. The scheduling includes two synthetic opioids—N-pyrrolidino isotonitazene and N-desethyl etonitazene—added to Schedule I of the 1961 Convention, and MDMB-FUBINACA, a synthetic cannabinoid added to Schedule II of the 1971 Convention. Countries are now required to apply control measures to these substances. The CND also confirmed maintaining coca leaf in Schedule I, preserving culturally protected traditional uses while addressing illicit cocaine production risks.

“The CND accepted the recommendation to include it in Schedule I of the 1961 Convention.”

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GovPing monitors WHO News for new healthcare & life sciences regulatory changes. Every update since tracking began is archived, classified, and available as free RSS or email alerts — 32 changes logged to date.

What changed

The CND accepted WHO recommendations to place N-pyrrolidino isotonitazene and N-desethyl etonitazene into Schedule I of the 1961 Single Convention on Narcotic Drugs, and MDMB-FUBINACA into Schedule II of the 1971 Convention on Psychotropic Substances. These substances have no recognized medical use and are associated with fatal overdoses and severe adverse effects. Separately, the CND confirmed maintaining coca leaf in Schedule I, acknowledging that traditional uses do not appear to pose significant public health risks while retaining controls to reduce illicit cocaine production risks.

Pharmaceutical manufacturers, importers, and exporters of these scheduled substances in countries party to the conventions must implement the required control measures. National regulatory authorities should review their schedules to ensure compliance with these international scheduling decisions. Traditional coca leaf users in Andean region countries with protected national frameworks are not affected by this confirmation.

Scheduled event

Date
2026-03-09

Archived snapshot

Apr 25, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

UN drug policy body acts on WHO recommendations to control new psychoactive substances and considers coca leaf review

23 April 2026 Departmental update Reading time:
Acting on recommendations from the World Health Organization (WHO) following the 48 th meeting of the WHO Expert Committee on Drug Dependence (ECDD), the United Nations Commission on Narcotic Drugs (CND) placed three harmful new psychoactive substances – one synthetic cannabinoid and two potent synthetic opioids, with no recognized medical use – under international control. As a result, countries are required to apply control measures to these substances in accordance with the international drug control conventions.

Strengthened control of high‑risk synthetic substances

The three harmful substances placed under international control are:

  • N -pyrrolidino isotonitazene, also referred to as isotonitazepyne, is a potent synthetic opioid associated with fatal and non‑fatal overdoses. It has been described as a crystalline solid and has been detected in falsified pharmaceutical products, appearing as coloured tablets. The CND accepted the recommendation to include it in Schedule I of the 1961 Convention.
  • N -desethyl etonitazene is a metabolite of etonitazene and a highly potent synthetic opioid linked to overdose deaths. It has been described as a crystalline solid, and a yellow or beige powder, and has appeared in falsified pharmaceutical opioid tablets. This substance was also placed into Schedule I of the 1961 Convention.
  • MDMB‑FUBINACA is a potent synthetic cannabinoid, typically appearing as a white powder, and has been associated with severe adverse effects and multiple cases of poisoning. It has been found sprayed onto herbal products and sold in e-liquids for vaping. The CND endorsed the recommendation to add it to Schedule II of the 1971 Convention on Psychotropic Substances. These scheduling decisions strengthen the global response to emerging synthetic substances that are clandestinely manufactured and associated with serious health risks, including fatalities, and for which no recognized medical use has been identified.

Current international control framework for coca leaf confirmed

The Commission also considered the WHO recommendation regarding coca leaf. Following a comprehensive scientific review, WHO had recommended maintaining coca leaf under Schedule I of the Single Convention on Narcotic Drugs. As it did not propose any change to the current international control status of coca leaf, no vote by the Commission was required.

WHO’s critical review of coca leaf, conducted for the first time in more than 30 years, brought updated scientific, cultural and public health evidence to the international arena. The ECDD acknowledged that traditional coca chewing and coca tea consumption do not appear to pose significant public health risks and that coca leaf holds important cultural meaning and traditional value for Indigenous Peoples across the Andean region.

At the same time, the Committee raised serious concerns about the rapidly expanding global cocaine market, increasing coca cultivation and the well‑documented ease and profitability of converting coca leaf into cocaine.

In this context, the ECDD concluded – and the CND confirmed – that retaining coca leaf in Schedule I of the 1961 Convention remains necessary to reduce the risks associated with illicit cocaine production, while still allowing countries to maintain culturally protected traditional uses within national legal frameworks. Legitimate medical, scientific and traditional uses of coca leaf, permitted under national legislation, remain unaffected.

WHO has encouraged further scientific research on coca leaf, including its long-term health effects and potential therapeutic properties.

WHO’s role in international drug control

Under the international drug control conventions, WHO is the only body mandated to conduct scientific and public health assessments of psychoactive substances. Through the ECDD, an independent scientific advisory body of international experts, the Organization evaluates available evidence on pharmacology, toxicology, epidemiology, dependence potential and therapeutic value of substances circulating globally, before making scheduling recommendations. These recommendations advise the CND, the United Nations’ policy-making body on international drug control, on whether international control measures are warranted to protect public health.

The decisions reflect WHO and the international community’s shared commitment to protecting public health, responding to evolving drug markets and ensuring that global policies remain firmly rooted in scientific assessment.

The WHO ECDD recommendations were endorsed by Member States at the 69 th session of the CND, held from 9 to 13 March 2026.

Media Contacts

Sarah Mascheroni

Communications officer
World Health Organization

Telephone: +41 22 791 2338 Mobile: +41 79 728 7311 Email: mascheronisa@who.int Related

Expert Committee on Drug Dependence

48 th ECDD meeting

Session 69 of the Commission on Narcotic Drugs

WHO’s work on drugs (psychoactive)

News

WHO Expert Committee concludes critical review of coca leaf, recommends maintaining current controls 10 December 2025 UN Commission approves WHO recommendations to place psychoactive substances under international control 13 March 2025 Fact sheets

Opioid overdose 29 August 2025

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Last updated

Classification

Agency
WHO
Published
April 23rd, 2026
Instrument
Notice
Branch
International
Legal weight
Non-binding
Stage
Final
Change scope
Substantive

Who this affects

Applies to
Government agencies Drug manufacturers Pharmaceutical companies
Industry sector
3254 Pharmaceutical Manufacturing
Activity scope
Drug scheduling International control compliance Substance control
Geographic scope
INT INT

Taxonomy

Primary area
Pharmaceuticals
Operational domain
Regulatory Affairs
Topics
Public Health International Trade

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