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Current as of January 02, 2024 | Updated by Findlaw Staff
(a) The manufacturer, packager, or distributor of any human use legend drug sold, delivered or offered for sale in the state must have printed on the label of the immediate container of the drug the name and address of the manufacturer, packager, or distributor of the finished dosage form of the drug.
(b) The pharmacist shall notify the patient of the substitution with a generic equivalent by noting the substitution on the prescription label.
(c) This section shall not apply to prescriptions dispensed for inpatients of a hospital, a nursing home or an assisted care living facility, as defined in § 68-11-201.
Cite this article: FindLaw.com - Tennessee Code Title 53. Food, Drugs and Cosmetics § 53-10-207 - last updated January 02, 2024 | https://codes.findlaw.com/tn/title-53-food-drugs-and-cosmetics/tn-code-sect-53-10-207/
FindLaw Codes may not reflect the most recent version of the law in your jurisdiction. Please verify the status of the code you are researching with the state legislature before relying on it for your legal needs.
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