1. (1) Drugs prepackaged by a pharmacy for later own use dispensing on prescription shall be in a container meeting USP standards and labeled to identify at a minimum:

   1. (a) Brand name, or generic name and manufacturer;
   2. (b) Strength;
   3. (c) Lot number;
   4. (d) Manufacturer’s expiration date, or any earlier date which, in the pharmacist’s professional judgment, is preferable.
2. (2) An internal control number which references manufacturer and lot number may be utilized.

Statutory/Other Authority

ORS 689

History

Renumbered from 855-041-0056, BP 7-2012, f. & cert. ef. 12-17-12
PB 6-1987, f. & ef. 5-1-87