217.819 Nonequivalent drug product formulary -- Distribution and revision.
136 words·~1 min read·
/ky/chapter-217/217-819A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
(1)The board shall prepare by regulation a nonequivalent drug product formulary of
drugs with their generic names for which there are no equivalent drug products, and
which should not be interchanged by pharmacists. The nonequivalent drug product
formulary shall list all drugs, drug products, and dosage formulations that the
United States Food and Drug Administration has determined to be therapeutically
nonequivalent.
(2)The board shall provide for annual distribution of copies of such formulary and
revisions and additions thereto among pharmacies licensed within the
Commonwealth and shall supply a copy to any person on request upon payment of
the price established by the board. Such formulary shall be revised and distributed
as often as new and pertinent information on drugs, drug products, and dosage
formulations becomes available from the United States Food and Drug
Administration.