Kratom-related opioid compounds appeared in flavored tablets and enhanced products. The DEA has now placed both in federal Schedule I. Know the names, the risks, and the law.
MGM-15, also called dihydro-7-hydroxymitragynine, and MGM-16, a fluorinated related compound, are chemically modified kratom-related opioids. Both were temporarily placed in Schedule I by the Drug Enforcement Administration, effective August 26, 2026, because the agency found an imminent hazard to public safety.
Ordinary retail sales of these substances are prohibited under federal law. A colorful package or an old online listing is not evidence that a product is lawful, currently available, or chemically verified.
These are not ordinary kratom powders. They are distinct, chemically modified compounds associated with opioid receptor activity and significant public-health concerns.
MGM-15 is dihydro-7-hydroxymitragynine, a chemically modified relative of 7-hydroxymitragynine (7-OH). It has opioid-receptor activity and is separately identified in the DEA's August 2026 order under drug code 9673.
MGM-16 is a fluorinated dihydro-7-hydroxymitragynine derivative, also described using 9-fluoro or 10-fluoro nomenclature depending on the numbering convention. It is separately controlled under DEA drug code 9674. It should not be confused with MGM-15 or mitragynine pseudoindoxyl.
Kratom leaf contains mitragynine and smaller amounts of 7-OH. MGM-15 and MGM-16 are chemically modified derivatives related to that alkaloid family, rather than ordinary whole-leaf kratom. Their manufacture and presence in any specific commercial product require evidence; the label alone is not proof.
No, not for ordinary retail sale in the United States. DEA's temporary Schedule I order took effect August 26, 2026, and is scheduled to run through August 26, 2028 unless extended or replaced. Unauthorized possession, manufacturing, and distribution are prohibited. Limited DEA-authorized activities such as research are subject to strict requirements. Read the federal order (91 FR 54948).
DEA identified these substances as posing an imminent hazard to public safety. Opioid-receptor activity raises concerns about sedation, impaired consciousness, respiratory depression, overdose, and dependence. However, controlled human studies specifically quantifying the effects and risks of MGM-15 and MGM-16 remain limited; do not treat marketing potency claims as established clinical comparisons.
Dependence and withdrawal are serious concerns for opioid-active compounds, including concentrated kratom-related products. The exact incidence, onset, and severity for MGM-15 and MGM-16 in humans are not well established. Someone using these products regularly should seek clinical advice rather than attempting an abrupt, unsupported withdrawal.
Archived product photographs show chewable tablets, flavored packaging, combination products, and terms such as “MGM,” “rapid release,” and “boosted.” Some labels may not distinguish MGM-15 from MGM-16. Images document marketing, not verified chemical composition or present-day availability.
Call 911 immediately for slow or absent breathing, inability to awaken, blue or gray lips, or collapse. Give naloxone if available, follow dispatcher instructions, and provide rescue breathing or CPR as directed. Naloxone may reverse opioid effects, but repeat doses or additional treatment may be needed. Do not leave the person alone. For nonemergency exposure guidance, call Poison Control at 1-800-222-1222.
Archived examples of products and advertising using MGM terminology. Their labels are not independent laboratory confirmation, and these images do not establish that the products remain available or lawful after federal scheduling.
The disturbing part is not just that MGM-15 exists. It is that kratom-derived opioid-like chemistry is being dressed up as fruit-flavored chewables, rapid-release extracts, and wellness alternatives while being sold in ordinary places.
The legal status and chemical identities above are grounded in the DEA's published temporary scheduling order. Medical risks are described conservatively because compound-specific human evidence is limited.
91 FR 54948–54956, Document 2026-17429. Defines MGM-15, MGM-16, and mitragynine pseudoindoxyl, and establishes their Schedule I controls.
Poison Help or 1-800-222-1222. Call 911 for life-threatening symptoms.