31A-48-102. Definitions. As used in this chapter: (1) (a) "Drug" means a substance that is: (i) (A) intended for use in the diagnosis, cure, mitigation, treatment, or prevention of disease in humans; and (B) recognized in or in a supplement to the official United States Pharmacopoeia, the Homeopathic Pharmacopoeia of the United States, or the official National Formulary; (ii) required by an applicable federal or state law or rule to be dispensed by prescription only; (iii) restricted to administration by practitioners only; (iv) a substance other than food intended to affect the structure or a function of the human body; or (v) intended for use as a component of a substance described in Subsection (1)(a)(i), (ii), (iii), or (iv). (b) "Drug" does not include a dietary supplement. (2) "Insurer" means the same as that term is defined in Section 31A-22-634. (3) "Manufacturer" means a person that is engaged in the manufacturing of a drug that is available for purchase by residents of the state. (4) "Rebate" means the same as that term is defined in Section 31A-46-102. (5) "Wholesale acquisition cost" means the same as that term is defined in 42 U.S.C. Sec. 1395w-3a.
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