Section 639.475 - Preparation and labeling of admixtures1. The managing pharmacist shall provide written guidelines for preparing parenteral admixture products to ensure that all pharmaceutical requirements are met.2. A label must be affixed to the container of any admixture. The label must include, but is not limited to: (a) The name of the patient for whom the admixture was prepared and the facility's or institution's identification of that patient;(b) The name and amount of the drugs added;(c) The name of the basic solution;(d) The name, initials or identifying code of the pharmacist who prepared or verified the admixture; and(e) The expiration date of the solution.Nev. Admin. Code § 639.475
Added to NAC by Bd. of Pharmacy, eff. 3-27-90; A 9-12-91NRS 639.070, 639.071, 639.072