Nine months in with the veterinary feed directive

Experiences and what is next

Authors

  • Michael D. Apley Department of Clinical Sciences, Kansas State University, Manhattan, KS 66506

DOI:

https://doi.org/10.21423/aabppro20173264

Keywords:

VFD, Guidance #213

Abstract

Last year at this time we were preparing for the Veterinary Feed Directive (VFD) transition and now we are survivors. There have been countless conversations between veterinarians and clients related to label indications, extralabel use, durations of use, concurrent use, repeated regimens (pulses), "hand fed” vs approved free choice feeds, and what comes next. We have advanced to the point of at least clarifying the uncertainties related to these subjects, and there is an indication of the next regulatory focus related to in-feed drugs. The "Blue Bird" labels have become familiar to many veterinarians to clarify the legal inclusions of Type C feeds. Also, Compliance Policy guide 615.115 has been useful for understanding the ability to use in-feed drugs in an extralabel manner in minor species. It is now clearly understood that asecond administration of an approved in-feed drug regimen to an animal requires an additional VFD be written. For determining which drugs may be concurrently fed together in feed, the Blue Bird labels and the Feed Additive Compendium are key sources. Next in the regulatory lineup is an evaluation of medically important in-feed antibiotics for which there is not a defined duration of administration in the label regimen.

Downloads

Published

2017-09-14

Issue

Section

General Sessions