N.D. Cent. Code § 4.1-43-02
This is the official text of N.D. Cent. Code § 4.1-43-02, part of North Dakota’s Cent. Code — part of the compiled statutory law of North Dakota, published by the state as "Cent. Code." Browse the sections below, each linked to its official government source.
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4.1-43-02. Registration of livestock medicine
Official statutory text
4.1-43-02. Registration of livestock medicine
The commissioner shall register any livestock medicine that does not violate this chapter,
upon the completion of an application by the manufacturer or distributor of the livestock
medicine and the payment of the registration fee prescribed in section 4.1-53-04. Registration of
livestock medicine is valid for a two-year period beginning July first and ending June thirtieth of
every even-numbered year unless it is canceled by the commissioner because a change is
made in the ingredients or formula of the livestock medicine or in the name, brand, or trademark
under which the medicine is sold. In the event of any change, the medicine must be registered
once again through an original application with the commissioner.
The certificate of registration must include a disclosure of the name and quantity or
proportion of each active ingredient and the names of the inert ingredients or fillers.
The commissioner shall register any livestock medicine that does not violate this chapter,
upon the completion of an application by the manufacturer or distributor of the livestock
medicine and the payment of the registration fee prescribed in section 4.1-53-04. Registration of
livestock medicine is valid for a two-year period beginning July first and ending June thirtieth of
every even-numbered year unless it is canceled by the commissioner because a change is
made in the ingredients or formula of the livestock medicine or in the name, brand, or trademark
under which the medicine is sold. In the event of any change, the medicine must be registered
once again through an original application with the commissioner.
The certificate of registration must include a disclosure of the name and quantity or
proportion of each active ingredient and the names of the inert ingredients or fillers.
Status: in_force · Read it on the official government site
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