Mycophenolate Mofetil EP Reference Standard from Japan
European Pharmacopoeia reference standard of mycophenolate mofetil used for analytical method validation and quality control testing. As a chemically defined aromatic heterocyclic compound, it precisely matches HTS 2934.99.01.00 specifications. Supplied in certified amounts (typically 100mg vials) for HPLC/GC calibration.
Duty Rate — Japan → United States
15%
Rate breakdown
9903.04.6215%Pharmaceuticals: patented pharma from JP/EU/KR/CH/LI — 15% floor rate
9903.05.900%Articles already subject to Section 232 (steel/aluminum/copper + derivatives, autos + parts, wood, medium/heavy vehicles + parts, semiconductors, patented pharma) — U.S. note 52(f)
Import Tips
• Include EP certificate confirming traceability to primary reference standard with assigned purity value
• Declare as 'reference standard for laboratory analysis only' to avoid pharmaceutical API scrutiny
• Small package exemption may apply for quantities <100g if properly documented as analytical reagent