Or. Admin. Code § 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;
(b)
Strength;
(c) Lot number;
(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.
Notes
Stat. Auth.: ORS 689
Stats. Implemented:
State regulations are updated quarterly; we currently have two versions available. Below is a comparison between our most recent version and the prior quarterly release. More comparison features will be added as we have more versions to compare.
No prior version found.