NAC639.781. Definitions.

As used in this section and NAC 639.784 and 639.788:

     1. “Original label” means the label affixed by an original pharmacy to the container of a controlled substance or dangerous drug.

     2. “Original pharmacy” means a pharmacy that dispenses a controlled substance or dangerous drug which is subsequently delivered to another pharmacy for repackaging.

     3. “Patient” means the ultimate user, patient or subject of research to whom a controlled substance or dangerous drug is dispensed by an original pharmacy. The term includes an agent of the patient.

     4. “Repackaging pharmacy” means a pharmacy that repackages a controlled substance or dangerous drug that was previously dispensed by another pharmacy.

     5. “Unit of use” has the meaning ascribed to it in NAC 639.460.

     (Added to NAC by Bd. of Pharmacy by R061-05, eff. 5-4-2006)