FDA Seeks Comments on Animal Drug Paperwork Again
Published Date: 6/18/2026
Notice
Summary
The FDA wants your thoughts on how they collect info about using drugs in animals in ways not originally approved (called extralabel use). This affects vets, farmers, and animal drug makers who report this info. You’ve got until August 17, 2026, to share your comments—no cost changes, just making sure the paperwork is clear and easy.
Analyzed Economic Effects
1 provisions identified: 0 benefits, 1 costs, 0 mixed.
Potential Method Development: 4,160-hour Burden
FDA may require analytical methods to detect residues from extralabel use of animal drugs under 21 CFR 530.22(b). FDA estimates up to two methods could be required each year, with an average burden of 4,160 hours per response and a total estimated 8,320 hours annually; comments are due by August 17, 2026 (OMB Control Number 0910-0325).
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