# Oral Dosage Form New Animal Drugs; Oxytetracycline
> **Food and Drug Administration** · Final rule. · Published 2006-06-27 · Effective 2006-06-27 · 71 FR 36483
## Document
- **Document number:** E6-10053
- **Category:** other
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 71 FR 36483
- **CFR reference:** 21 CFR 520
- **Publication date:** 2006-06-27
- **Effective date:** 2006-06-27
## 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 Pfizer, Inc. The supplemental NADA revises labeling of oxytetracycline soluble powder with the current genus for the causative bacteria for American foul brood of honeybees.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2006/06/27/E6-10053/oral-dosage-form-new-animal-drugs-oxytetracycline)
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