Nevada Code § 577.100

Establishment of program concerning veterinary feed directives; registration of animal remedies, veterinary biologics and pharmaceuticals; application for registration; regulations
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1. The Department may establish, by
regulation, a program to implement the requirements of federal regulations
concerning veterinary feed directives, as defined in 21 U.S.C. 354,
including, without limitation, requirements for the registration of any animal
remedy, veterinary biologic or pharmaceutical, as those terms are defined in
those federal regulations.
2. The regulations adopted by the
Department pursuant to subsection 1 must provide that:
(a) Except as otherwise provided in this
paragraph, no person shall sell, offer or expose for sale, or deliver to a
user, an animal remedy, veterinary biologic or pharmaceutical, in package or in
bulk, which has not been registered with the Department pursuant to this
chapter and the regulations adopted pursuant thereto. Any product registered
pursuant to chapter 586 of NRS or under the
Federal Insecticide, Fungicide, and Rodenticide Act, 7 U.S.C. 136 et seq.,
is not subject to the provisions of this chapter and the regulations adopted
pursuant thereto.
(b) Except as otherwise provided by law, the
manufacturer of each brand of animal remedy, veterinary biologic and
pharmaceutical to be sold in this State, whether in package or in bulk, shall
register such products with the Department annually pursuant to this chapter
and the regulations adopted pursuant thereto. The regulations may authorize a
manufacturer who sells more than one animal remedy, veterinary biologic or
pharmaceutical in this State to register all such products with one
application.
(c) An application for registration of an animal
remedy, veterinary biologic or pharmaceutical must be made on forms provided by
the Department and must be accompanied by a reasonable annual registration fee
established by the Department by regulation for each animal remedy, veterinary
biologic and pharmaceutical.
(d) An application pursuant to paragraph (c)
must:
(1) Be filed on or before July 1 of each
year; and
(2) Include a list of all animal remedies,
veterinary biologics and pharmaceuticals that the applicant intends to market
in this State during the following fiscal year.

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