217.819 Nonequivalent drug product formulary -- Distribution and revision. (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 <br>which should not be interchanged by pharmacists. The nonequivalent drug product <br>formulary shall list all drugs, drug products, and dosage formulations that the <br>United States Food and Drug Administration has determined to be therapeutically <br>nonequivalent. (2) The board shall provide for annual distribution of copies of such formulary and revisions and additions thereto among pharmacies licensed within the <br>Commonwealth and shall supply a copy to any person on request upon payment of <br>the price established by the board. Such formulary shall be revised and distributed <br>as often as new and pertinent information on drugs, drug products, and dosage <br>formulations becomes available from the United States Food and Drug <br>Administration. Effective: July 15, 1982 <br>History: Amended 1982 Ky. Acts ch. 399, sec. 2, effective July 15, 1982. -- Created 1972 Ky. Acts ch. 126, sec. 6.
217.819 Nonequivalent drug product formulary -- Distribution and revision. (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 <br>which should not be interchanged by pharmacists. The nonequivalent drug product <br>formulary shall list all drugs, drug products, and dosage formulations that the <br>United States Food and Drug Administration has determined to be therapeutically <br>nonequivalent. (2) The board shall provide for annual distribution of copies of such formulary and revisions and additions thereto among pharmacies licensed within the <br>Commonwealth and shall supply a copy to any person on request upon payment of <br>the price established by the board. Such formulary shall be revised and distributed <br>as often as new and pertinent information on drugs, drug products, and dosage <br>formulations becomes available from the United States Food and Drug <br>Administration. Effective: July 15, 1982 <br>History: Amended 1982 Ky. Acts ch. 399, sec. 2, effective July 15, 1982. -- Created 1972 Ky. Acts ch. 126, sec. 6.
217.819 Nonequivalent drug product formulary -- Distribution and revision. (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 <br>which should not be interchanged by pharmacists. The nonequivalent drug product <br>formulary shall list all drugs, drug products, and dosage formulations that the <br>United States Food and Drug Administration has determined to be therapeutically <br>nonequivalent. (2) The board shall provide for annual distribution of copies of such formulary and revisions and additions thereto among pharmacies licensed within the <br>Commonwealth and shall supply a copy to any person on request upon payment of <br>the price established by the board. Such formulary shall be revised and distributed <br>as often as new and pertinent information on drugs, drug products, and dosage <br>formulations becomes available from the United States Food and Drug <br>Administration. Effective: July 15, 1982 <br>History: Amended 1982 Ky. Acts ch. 399, sec. 2, effective July 15, 1982. -- Created 1972 Ky. Acts ch. 126, sec. 6.
