31A-48-102. Definitions.
210 words·~1 min read·
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Effective 5/4/2022
31A-48-102. Definitions.
As used in this chapter:
(a)"Drug" means a substance that is:
(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.
Amended by Chapter 198 , 2022 General Session