1. (1) In accordance with Subsections 58-17b-601(1) and 58-17b-610.8, the operating standards for prescription devices are established in this section.
2. (2) The prescribing practitioner identified on the prescription document under Subsection 58-17-610.8(1) is the prescriber for the prescription device described in Subsection 58-17b-610.8(3).

3. (3) The pharmacist or pharmacy intern dispensing the prescription device shall determine the following:

   1. (a) an appropriate dispense quantity;
   2. (b) directions for device use; and
   3. (c) refill.

4. (4) Each prescription device dispensed by a pharmacist or pharmacy intern shall be:

   1. (a) dispensed in accordance with Subsection 58-17b-602(1)(a) through (e) and Section 58-17b-609; and
   2. (b) dispensed from a Class A or Class B pharmacy.

5. (5)(a) Notice of the prescription device dispense shall be conveyed to the prescribing practitioner in writing, by electronic transmission, or by telephone within five business days following the prescription device dispense.

   1. (b) The prescription device dispense notice shall include the following:

      1. (i) pharmacy name;
      2. (ii) pharmacy phone number;
      3. (iii) patient;
      4. (iv) dispensed quantity;
      5. (v) directions for use; and
      6. (vi) refill.

KEY: pharmacists, licensing, pharmacies

Date of Last Change: August 8, 2025

Notice of Continuation: August 5, 2024

Authorizing, and Implemented or Interpreted Law: 63G-3-201; 58-17b-101; 58-17b-601(1); 58-37-1; 58-1-106(1)(a); 58-1-202(1)(a)