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AS 08.80.294

Information about equivalent generic drugs and interchangeable biological products

Known as the Pharmacy Act

The act spans §§ 08.80.003 to 08.80.490 (61 sections).

(a) In addition to other information that may be required under state or federal laws or regulations, a pharmacist, when dispensing a brand-name prescription drug order that is (1) not a biological product, shall include the generic drug name that is an equivalent drug product for the drug dispensed;

(2) a biological product, shall include the dispensed product's (A) proprietary name, if available; or

(B) proper name.

(b) The generic drug name or proprietary or proper biological product name required under (a) of this section shall be placed directly on the container's label near the brand name.

(c) In this section, (1) “proper name” means a name that reflects scientific characteristics of the product such as chemical structure and pharmacological properties;

(2) “proprietary name” means a name that is trademarked and registered for private use.

Official source: Alaska State Legislature. Reproduced from public-domain Alaska statutes; confirm against the official source for the current text. Not legal advice.