# Oral Dosage Form New Animal Drugs; Oxytetracycline Hydrochloride Soluble Powder
> **Food and Drug Administration** · Final rule. · Published 2006-07-05 · Effective 2006-07-05 · 71 FR 38072
## Document
- **Document number:** E6-10445
- **Category:** other
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 71 FR 38072
- **CFR reference:** 21 CFR 520
- **Publication date:** 2006-07-05
- **Effective date:** 2006-07-05
## Abstract

The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of an abbreviated new animal drug application (ANADA) filed by V[eacute]toquinol NA, Inc. The ANADA provides for use of oxytetracycline soluble powder to prepare medicated drinking water for the treatment of various bacterial diseases of livestock.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2006/07/05/E6-10445/oral-dosage-form-new-animal-drugs-oxytetracycline-hydrochloride-soluble-powder)
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