88R3067 JG-D     By: Klick H.B. No. 4332       A BILL TO BE ENTITLED   AN ACT   relating to the redistribution of donated prepackaged prescription   drugs.          BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF TEXAS:          SECTION 1.  Section 442.001, Health and Safety Code, is   amended by adding Subdivision (6-a) to read as follows:                (6-a) "Prepackage" means the act of repackaging and   relabeling varying quantities of prescription drugs from a   manufacturer's original commercial container into a prescription   container, unit-dose packaging, or a multi-compartment container   for a pharmacist to dispense to a consumer.          SECTION 2.  Subchapter B, Chapter 442, Health and Safety   Code, is amended by adding Section 442.0515 to read as follows:          Sec. 442.0515.  REDISTRIBUTION OF DONATED PREPACKAGED   PRESCRIPTION DRUGS. (a) A participating provider may dispense to a   recipient donated prescription drugs that are prepackaged and   labeled in accordance with this section and rules adopted by the   Texas State Board of Pharmacy.          (b)  A prepackaged prescription drug a participating   provider dispenses to a recipient must contain a label that   includes:                (1)  the drug's brand name or, for a generic version of   the drug, the drug's generic name and the manufacturer or   distributor of the drug;                (2)  the amount of the drug in a given dose;                (3)  the drug's lot number;                (4)  the earliest expiration date of the drug for that   drug lot number; and                (5)  the quantity of any drug the provider dispenses in   more than one dose.          (c)  A participating provider shall maintain a record of each   prepackaged prescription drug dispensed to a recipient. The record   must include:                (1)  the drug's name, the amount of the drug in a given   dose, and the dosage size or frequency;                (2)  the provider's lot number for that drug;                (3)  the drug's manufacturer or distributor;                (4)  the manufacturer's lot number for that drug;                (5)  the expiration dates of the drug from that drug's   lot number;                (6)  the quantity of the drug in each prepackaged unit;                (7)  the number of prepackaged units that include the   drug;                (8)  the date the drug was prepackaged;                (9)  the name, initials, or written or electronic   signature of the individual who prepackaged the drug; and                (10)  the written or electronic signature of the   pharmacist responsible for the drug's prepackaging.          SECTION 3.  As soon as practicable after the effective date   of this Act, the Texas State Board of Pharmacy shall adopt any rules   necessary to implement the changes in law made by this Act.          SECTION 4.  This Act takes effect September 1, 2023.