37-7-502. Definitions. As used in this part, the following definitions apply:
     (1) "Bioavailability" means the extent and rate of absorption from a dosage form as reflected by the time-concentration curve of the administered drug in the systemic circulation.
     (2) "Bioequivalent" means a chemical equivalent which, when administered to the same individual in the same dosage regimen, will result in comparable bioavailability.
     (3) "Brand name" means the proprietary or the registered trademark name given to a drug product by its manufacturer, labeler, or distributor and placed upon the drug, its container, label, or wrapping at the time of packaging.
     (4) "Chemical equivalent" means drug products that contain the same amounts of the same therapeutically active ingredients in the same dosage forms and that meet present compendium standards.
     (5) "Drug product" means a dosage form containing one or more active therapeutic ingredients along with other substances included during the manufacturing process.
     (6) "Generic name" means the chemical or established name of a drug product or drug ingredient published in the latest edition of the official United States Pharmacopoeia/National Formulary.
     (7) "Person" means an individual, firm, partnership, association, corporation, or any other entity, whether organized for profit or not.
     (8) "Prescriber" means a practitioner licensed under the professional laws of the state to administer medicine and drugs.
     (9) "Present compendium standard" means the official standard for drug excipients and drug products listed in the latest revision of the United States Pharmacopoeia/National Formulary.
     (10) "Product selection" means to dispense without the prescriber's express authorization a different drug product in place of the drug product prescribed.
     (11) "Therapeutically equivalent" means those chemical equivalents which, when administered in the same dosage regimen, will provide essentially the same therapeutic effect as measured by the control of a symptom or a disease and/or toxicity.

     History: En. 66-1529 by Sec. 2, Ch. 403, L. 1977; R.C.M. 1947, 66-1529; amd. Sec. 11, Ch. 379, L. 1981.