Animal Drugs, Feeds, and Related Products; Neomycin Sulfate Soluble Powder
other · US Department of Health and Human Services · Rule · Published 1996-06-20 · Effective 1996-06-20 · 61 FR 31398
Document
Document number
96-15724
Federal Register citation
61 FR 31398
CFR reference
21 CFR 520
Type
Rule
Action
Final rule.
Category
other
Sub-agency
US Department of Health and Human Services
Publication date
1996-06-20
Effective date
1996-06-20
Abstract
The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of a supplemental new animal drug application (NADA) filed by The Upjohn Co. and two supplemental abbreviated new animal drug applications (ANADA's), one filed by Pfizer, Inc., and the other filed by Rhone Merieux, Inc. The applications provide for use of neomycin sulfate soluble powder in drinking water or in milk for cattle (excluding veal calves), swine, sheep, and goats for the treatment and control of colibacillosis. The supplements provide for revised preslaughter withdrawal times following use of the drug and revised tolerances for neomycin residues in edible tissues of treated animals.