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
27.5%
Rate breakdown
9903.04.6215%Patented pharmaceutical articles that are the product of Japan, of a European Union member country, of South Korea, of Switzerland, or of Liechtenstein as provided for in subdivisions (c) and (f) of U.S. note 40 to this subchapter
9903.05.4912.5%Except for products described in headings 9903.05.85–9903.05.92, articles the product of Japan, with an ad valorem (or ad valorem equivalent) rate of duty under column 1 less than 12.5 percent, as provided for in U.S. note 52 to this subchapter
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