Nebraska § 71-2411 Terms, defined

Nebraska Statutes

§ 71-2411 — Terms, defined

Nebraska § 71-2411

Ch. 71Public Health and Welfare

This text of Nebraska § 71-2411 (Terms, defined) is published on Counsel Stack Legal Research, covering Nebraska primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook

Neb. Rev. Stat. § 71-2411 (2026).

Text

For purposes of the Emergency Box Drug Act:

(1)Authorized personnel means any medical doctor, doctor of osteopathy, registered nurse, licensed practical nurse, nurse practitioner, pharmacist, or physician assistant;

(2)Calculated expiration date has the same meaning as in section 38-2808.01 ;

(3)Department means the Department of Health and Human Services;

(4)Drug means any prescription drug or device or legend drug or device defined under section 38-2841 , any nonprescription drug as defined under section 38-2829 , any controlled substance as defined under section 28-405 , or any device as defined under section 38-2814 ;

(5)Emergency box drugs means drugs required to meet the immediate therapeutic needs of patients when the drugs are not available from any other authorized sourc

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For purposes of the Emergency Box Drug Act:
(1) Authorized personnel means any medical doctor, doctor of osteopathy, registered nurse, licensed practical nurse, nurse practitioner, pharmacist, or physician assistant;
(2) Calculated expiration date has the same meaning as in section 38-2808.01 ;
(3) Department means the Department of Health and Human Services;
(4) Drug means any prescription drug or device or legend drug or device defined under section 38-2841 , any nonprescription drug as defined under section 38-2829 , any controlled substance as defined under section 28-405 , or any device as defined under section 38-2814 ;
(5) Emergency box drugs means drugs required to meet the immediate therapeutic needs of patients when the drugs are not available from any other authorized source in time to sufficiently prevent risk of harm to such patients by the delay resulting from obtaining such drugs from such other authorized source;
(6) Long-term care facility means an intermediate care facility, an intermediate care facility for persons with developmental disabilities, a long-term care hospital, a mental health substance use treatment center, a nursing facility, or a skilled nursing facility, as such terms are defined in the Health Care Facility Licensure Act;
(7) Multiple dose vial means any bottle in which more than one dose of a liquid drug is stored or contained;
(8) NDC means the National Drug Code published by the United States Food and Drug Administration;
(9) Pharmacist means a pharmacist as defined in section 38-2832 who is employed by a supplying pharmacy or who has contracted with a long-term care facility to provide consulting services; and
(10) Supplying pharmacy means a pharmacy that supplies drugs for an emergency box located in a long-term care facility. Drugs in the emergency box are owned by the supplying pharmacy.

Legislative History

Source: Laws 1994, LB 1210, § 183; Laws 1996, LB 1044, § 625; Laws 1997, LB 608, § 16; Laws 2000, LB 819, § 106; Laws 2001, LB 398, § 70; Laws 2007, LB296, § 540; Laws 2007, LB463, § 1194; Laws 2009, LB195, § 69; Laws 2013, LB23, § 34; Laws 2018, LB1034, § 63; Laws 2020, LB1052, § 9. Cross References: Health Care Facility Licensure Act, see section 71-401.