1. (1) All prescription drugs shall be in an appropriate container bearing a label in conformance with federal law.
2. (2) For parenteral admixtures, the label shall include the date and time of the addition or the beyond use date.
3. (3) For prepackaged products, the label shall include an expiration date that is the lesser of the manufacturer’s original expiration date, one (1) year from the date the drug is prepackaged, or a shorter period if warranted.
4. (4) For repackaged drugs, the label shall include the prescription number and contact information for the original dispensing pharmacy, a statement indicating that the drug has been repackaged, and contact information for the repackager.

[54-1736, added 2025, ch. 93, sec. 38, p. 435.]