# Oral Dosage Form New Animal Drugs; Oxytetracycline Hydrochloride Soluble Powder
> **Food and Drug Administration** · Final rule. · Published 1999-09-07 · Effective 1999-09-07 · 64 FR 48543
## Document
- **Document number:** 99-23131
- **Category:** other
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 64 FR 48543
- **CFR reference:** 21 CFR 520
- **Publication date:** 1999-09-07
- **Effective date:** 1999-09-07
## 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 Phoenix Scientific, Inc. The supplemental ANADA provides for an additional package size of oxytetracycline hydrochloride soluble powder to be used to make a medicated drinking water for chickens, turkeys, cattle, swine, and sheep for control and/or treatment of various bacterial diseases. EFFECTIVE DATE: September 7, 1999.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/1999/09/07/99-23131/oral-dosage-form-new-animal-drugs-oxytetracycline-hydrochloride-soluble-powder)
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