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DEA Revises Emergency Opioid Scheduling for Concentrated Kratom Products

New federal notices use concentration and ratio thresholds to distinguish enhanced opioid products from trace amounts in botanical kratom.

The Drug Enforcement Administration is revising its emergency scheduling approach for 7-hydroxymitragynine and three related opioid substances, using concentration thresholds intended to separate enhanced products from trace compounds found in botanical kratom.

The agency will issue new notices of intent covering 7-OH, mitragynine pseudoindoxyl, MGM-15 and MGM-16. The change follows updated scientific advice from the Department of Health and Human Services and is procedural rather than a final scheduling order for every substance.

Under the recommendation, 7-OH and MGPI would be subject to Schedule I control when either substance, or their combined amount, exceeds one milligram per gram in a solid product or one milligram per milliliter in a liquid. The same treatment would apply when the ratio of mitragynine to 7-OH, MGPI or their combined amount is below 100 to one.

Those thresholds reflect a legal and scientific problem. Low levels of 7-OH occur naturally in kratom, and HHS said MGPI may also appear in trace amounts. A rule aimed only at the names of the substances could therefore reach ordinary botanical material along with products deliberately fortified to produce a stronger opioid effect.

MGPI, MGM-15 and MGM-16 were temporarily placed in Schedule I in August. Those controls remain in force during the new 30-day notice period and until the DEA issues another temporary scheduling order. The agency has not yet issued a temporary scheduling order for 7-OH.

The Justice Department’s scheduling announcement explains the thresholds and the different procedural status of the four substances.

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