N.Y. Comp. Codes R. & Regs. tit. 1 § 59.3

Current through Register Vol. 46, No. 50, December 11, 2024

Section 59.3 - Report to the commissioner

(a) As provided by subdivision 3 of section 89 of the Agriculture and Markets Law, every individual, firm, corporation or institution preparing or selling or receiving for retention or sale or giving away within this State any therapeutic preparation of microbiological origin for use in the detection, prevention, control or eradication of infectious or contagious diseases of domestic animals or fowls, or for the administration thereto for whatever purpose, shall report to the commissioner the character and purpose of the preparation, the quantity, the name and address of the manufacturer, and the name and address of the person or firm to whom the product was sold or given away.

(b) All such preparations except the following are exempt from this section:

(1) Anaplasmosis antigen and vaccine;

(2) Anthrax vaccine;

(3) Blue tongue vaccine;

(4) Brucella abortus vaccine (bovine abortion vaccine);

(5) Brucella abortus antigen;

(6) Encephalitis (encephalomyelitis) vaccine (avian);

(7) Equine infectious anemia antigen (swamp fever antigen);

(8) Gumboro (bursal) disease vaccine;

(9) Hog cholora virus, vaccine;

(10) Marek's disease vaccine;

(11) Mycoplasma gallisepticum antigen and positive serum;

(12) Mycoplasma synoviae antigen and positive serum;

(13) Pseudorabies vaccine, both modified live and killed types; and

(14) All other biological products which are developed for the prevention of animal or poultry diseases after the effective date of this Part and which contain a living pathogenic agent.

N.Y. Comp. Codes R. & Regs. Tit. 1 § 59.3