1.  The provisions of this chapter and any regulations adopted pursuant thereto do not apply to:

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(a) A veterinary biologic product that is:

(1) Licensed for production under a product license; and

(2) Directly marketed by a manufacturing facility holding an establishment license for administration to livestock.

(b) A pharmaceutical technician of the Armed Forces of the United States or a pharmaceutical technician of any division or department of the United States in the discharge of his or her official duties, including, without limitation, providing care in a hospital in accordance with an agreement entered into pursuant to NRS 449.2455.

2.  As used in this section:

(a) ’Establishment license’ means a U. S. Veterinary Biologics Establishment License issued by the Administrator of the Animal and Plant Health Inspection Service of the United States Department of Agriculture pursuant to the Virus-Serum-Toxin Act, 21 U.S.C. § 151 to 159, inclusive, and any amendments to or replacements of the Act, and any regulations adopted pursuant to the Act.

(b) ’Livestock’ has the meaning ascribed to it in subsections 1 and 3 to 6, inclusive, of NRS 571.022.

(c) ’Product license’ means a U. S. Veterinary Biological Product License issued by the Administrator of the Animal and Plant Health Inspection Service of the United States Department of Agriculture pursuant to the Virus-Serum-Toxin Act, 21 U.S.C. § 151 to 159, inclusive, and any amendments to or replacements of the Act, and any regulations adopted pursuant to the Act.

(d) ’Veterinary biologic product’ has the meaning ascribed to ‘biological product’ in 9 C.F.R. § 101.2.