As used in the Wholesale Prescription Drug Importation Act:

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A. “Canadian supplier” means a manufacturer, wholesale distributor or pharmacy that is appropriately licensed or permitted under Canadian federal or provincial laws and rules to manufacture, distribute or dispense prescription drugs;

B. “committee” means the prescription drug importation advisory committee;

C. “department” or “authority” means the health care authority department; D. “eligible prescription drug” means a drug eligible for importation that:

(1)     meets the United States food and drug administration’s standards related to safety, effectiveness, misbranding and adulteration;

(2)     does not violate federal patent laws;

(3)     is expected to generate cost savings; and

(4)     is not a controlled substance;

E. “program” means the wholesale prescription drug importation program; and

F. “state drug wholesaler” means a licensed wholesale drug distributor that contracts with the state to import eligible prescription drugs from a Canadian supplier.