Extra
Label Drug Use in Animals: FDA Final Rule The Food and Drug Administration (FDA) has issued a final
rule to allow veterinarians to prescribe extra label uses of
certain approved animal drugs and approved human drugs for animals
(Federal Register, November 7, 1996, Volume 61, Number 217 pg
57731)
Revised Guidelines
for Evaluating Mastitis Products The Food and Drug Administration (FDA) announced the availability of the revised
guidance document entitled Target Animal Safety and Drug Effectiveness Studies
for Anti-Microbial Bovine Mastitis Products (Lactating and Non-lactating Cow
Products) prepared by the Center for Veterinary Medicine (Federal Register, April
29, 1996, Volume 61, Number 83, pg 18747)
Draft Guideline for
Teat Antiseptic Product Development This Food and Drug Administration (FDA)
guideline outlines the regulatory requirements and procedures for evaluating
products considered for approval (published February, 1993)
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