Ephedra extract, derived from Ephedra sinica and related species, contains ephedrine alkaloids that are subject to strict DEA and FDA regulatory controls in the United States. The sole 10-digit line 1302140100 covers all forms of ephedra sap and extract, and importers must navigate both DEA List I chemical regulations — which govern ephedrine and pseudoephedrine as precursors to controlled substances — and FDA restrictions on ephedra-containing dietary supplements. The absence of top-country data for this heading reflects the narrow and tightly monitored nature of licit trade flows. Classification and admissibility are highly complex; consult a licensed customs broker and regulatory counsel before attempting any import.
AI-written summary of the official U.S. Census Bureau trade figures on this page — verify before relying on it.
Ephedra extracts contain ephedrine and pseudoephedrine, which are DEA List I chemicals — meaning they are recognized precursors to methamphetamine and other controlled substances. Importers must register with DEA and comply with import quota and reporting requirements for these chemicals, separate from and in addition to FDA's restrictions on ephedra in dietary supplements. Both regulatory frameworks must be satisfied before a shipment can legally enter US commerce.
Licit importation for pharmaceutical-grade ephedrine synthesis is possible but requires DEA importer registration, compliance with annual import quotas set by DEA, and FDA oversight of the downstream manufacturing process. The regulatory burden is substantial, and any deviation from approved use can result in seizure and significant penalties. Engaging DEA-registered legal counsel and a licensed customs broker with controlled-substance experience is essential.
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12-mo low · imports
YoY · ProFewer than 6 of the last 12 months reported trade above $500K; the trend chart is not shown for thin series.
Through December 2024. Source: U.S. Census Bureau.
Imports · December 2024
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