Current through Register Vol. 63, No. 12, December 1, 2024
Section 855-041-1135 - Defines Labeling and Container Requirements for Repackage Drugs(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: (a) Brand name, or generic name and manufacturer;(d) Manufacturer's expiration date, or any earlier date which, in the pharmacist's professional judgment, is preferable.(2) An internal control number which references manufacturer and lot number may be utilized.Or. Admin. Code § 855-041-1135
PB 6-1987, f. & ef. 5-1-87); Renumbered from 855-041-0056, BP 7-2012, f. & cert. ef. 12-17-12Stat. Auth.: ORS 689
Stats. Implemented: