Tennessee Statutes
§ 53-10-207 — Contents of label
Tennessee § 53-10-207
JurisdictionTennessee
Title53
This text of Tennessee § 53-10-207 (Contents of label) is published on Counsel Stack Legal Research, covering Tennessee primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.
Bluebook
Tenn. Code Ann. § 53-10-207 (2026).
Text
(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 .
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Legislative History
Acts 2005, ch. 434, § 9.
Nearby Sections
15
§ 53-1-101
Administration - Short title§ 53-1-102
Chapter definitions§ 53-1-103
Prohibited acts - Penalties - Exceptions§ 53-1-104
Food deemed adulterated§ 53-1-105
Food deemed misbranded§ 53-1-108
Drugs or devices deemed adulterated§ 53-1-110
Sale of new drugs§ 53-1-111
Cosmetics deemed adulterated§ 53-1-112
Cosmetics deemed misbranded§ 53-1-113
False advertising§ 53-1-114
Exemptions from labeling requirementsCite This Page — Counsel Stack
Bluebook (online)
Tennessee § 53-10-207, Counsel Stack Legal Research, https://law.counselstack.com/statute/tn/53-10-207.