# Animal Drugs, Feeds, and Related Products; Neomycin Sulfate Soluble Powder
> **US Department of Health and Human Services** · Final rule. · Published 1996-06-20 · Effective 1996-06-20 · 61 FR 31398
## Document
- **Document number:** 96-15724
- **Category:** other
- **Sub-agency:** US Department of Health and Human Services
- **Federal Register citation:** 61 FR 31398
- **CFR reference:** 21 CFR 520
- **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.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/1996/06/20/96-15724/animal-drugs-feeds-and-related-products-neomycin-sulfate-soluble-powder)
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