{"data":{"id":"us-ky/krs-217.895","jurisdiction":"us-ky","citation":"KRS 217.895","heading":"Inspections -- Records of pharmacy.","body":"(1) Routine inspections of pharmacies for compliance with KRS 217.815 to 217.826\nshall be undertaken by the Kentucky Board of Pharmacy.\n(2) Every pharmacy shall retain for a period of two (2) years from July 15, 1982, a\npharmacy record of all prescribed drug a nd biological products dispensed. The\npharmacy record shall be retained for the purpose of providing valid data for bona\nfide research and reporting to the General Assembly as to the effectiveness of KRS\n217.815 to 217.826. The pharmacy record shall include:\n(a) The brand name of the drug or biological product, when applicable.\n(b) The name of the manufacturer or the supplier of the drug or biological\nproduct, if the drug or biological product has no brand name.\n(c) The strength of the drug or biological product, when significant.\n(d) The quantity dispensed, when applicable.\n(e) The serial number of the prescription.\n(f) The date the prescription was originally dispensed and refilled.\n(g) The name of prescribing practitioner.\n(h) The name of patient for whom the drug or biological product was prescribed.\n(i) The price for which the drug or biological product was sold to the purchaser.\n(j) A notation if the practitioner indicated \"Do not substitute\" or the purchaser\nrefused the product selected.","path":["KRS Chapter 217"],"source_url":"https://apps.legislature.ky.gov/law/statutes/statute.aspx?id=45077","current_through":"Includes enactments through the 2026 Regular Session","vintage":"09/05/2026","retrieved_at":"2026-09-05T20:52:27Z","sha256":"1afcfe9c51ce3eb4a16a01eb712c0af60d4847cb19afd4ad725628c32e1a08e1","source_id":"us-ky","stale":false,"prev":"us-ky/krs-217.894","next":"us-ky/krs-217.896"},"notice":"GroundRules: Original legal text. Not legal advice."}