Sterile Mycophenolate Mofetil for Injection Formulation from Mexico
Sterile-grade mycophenolate mofetil powder intended for IV injection formulation after further processing. Classified under HTS 2934.99.01.00 as bulk aromatic heterocyclic API despite sterile processing, per Chapter 29 notes excluding only finished medicaments. Meets parenteral quality standards with endotoxin limits <0.5 EU/mg.
Duty Rate — Mexico → United States
110%
Rate breakdown
9903.04.60100%Except as provided in heading 9903.04.61, patented pharmaceutical articles as provided for in subdivisions (c) and (d) of U.S. note 40 to this subchapter
9903.05.5510%Except for products described in headings 9903.05.85–9903.05.92 and 9903.05.94, articles the product of Mexico, as provided for in U.S. note 52 to this subchapter
Import Tips
• Provide bacterial endotoxin test results and sterility assurance documentation for parenteral use
• Nitrogen purged containers required to prevent oxidative degradation during ocean transit
• Particle size distribution data critical for injection formulation compatibility