# Oral Dosage Form New Animal Drugs; Oxytetracycline Powder
> **Food and Drug Administration** · Final rule. · Published 2006-12-08 · Effective 2006-12-08 · 71 FR 71038
## Document
- **Document number:** E6-20928
- **Category:** other
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 71 FR 71038
- **CFR reference:** 21 CFR 520
- **Publication date:** 2006-12-08
- **Effective date:** 2006-12-08
## Abstract

The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of a supplemental abbreviated new animal drug application (ANADA) filed by IVX Animal Health, Inc. The supplemental ANADA revises labeling of generic oxytetracycline soluble powder with the current scientific names of the causative bacteria of foulbrood of honeybees.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2006/12/08/E6-20928/oral-dosage-form-new-animal-drugs-oxytetracycline-powder)
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