166D.14 Pseudorabies immunization products.
1. A person shall not use, sell, or distribute or offer to sell or distribute a pseudorabies immunization product within the state unless the products are approved by the secretary. However, the secretary shall approve a pseudorabies immunization product for purposes of product research or testing by a biological laboratory, government authority, or manufacturer of biological products if the secretary concludes that the use will not be detrimental to the state pseudorabies disease program.
2. Only a licensed veterinarian may buy and dispense a department-approved immunization product. The veterinarian must report information relating to the use of the product to the department, including the name and address of the owner and the number of doses used. The report shall be signed by the owner or the owner’s agent. The report shall be mailed to the department immediately after the use of the product.
3. A differentiable vaccinate to be classified as a noninfected animal must react negatively to field strains of pseudorabies virus as determined by a companion differentiable serologic test. The swine must be identified as differentiable vaccinated animals.
89 Acts, ch 280, §14; 2017 Acts, ch 54, §76
Referred to in §166D.10
Structure Iowa Code
Chapter 166D - PSEUDORABIES CONTROL
Section 166D.1 - Purpose — rules.
Section 166D.3 - State pseudorabies advisory committee.
Section 166D.3A - Departmental determination of pseudorabies prevalence.
Section 166D.6 - Reporting of test results.
Section 166D.7 - Noninfected herds.
Section 166D.8 - Infected herds.
Section 166D.9 - Quarantined herds.
Section 166D.10 - Movement of swine.
Section 166D.10A - Restricted movement — requirements.
Section 166D.10B - Approved premises.
Section 166D.11 - Vaccination and testing requirements.
Section 166D.12 - Concentration points.
Section 166D.13 - Exhibition of swine.
Section 166D.14 - Pseudorabies immunization products.
Section 166D.15 - Tracing pseudorabies to source or destination herds.