# Oral Dosage Form New Animal Drugs; Oxytetracycline Hydrochloride Soluble Powder
> **Food and Drug Administration** · Final rule. · Published 1996-10-08 · Effective 1996-10-08 · 61 FR 52690
## Document
- **Document number:** 96-25811
- **Category:** other
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 61 FR 52690
- **CFR reference:** 21 CFR 520
- **Publication date:** 1996-10-08
- **Effective date:** 1996-10-08
## 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 Phoenix Scientific, Inc. The supplemental ANADA provides for an additional container size for the firm's oxytetracycline hydrochloride (OTC HCl) soluble powder. The drug product is administered orally in drinking water for either control or control and treatment of certain diseases of chickens, turkeys, swine, cattle, and sheep. In addition, the regulations are amended to specify the withdrawal period for use of medicated drinking water made from the subject sponsor's drug and to add certain warning statements required on the labeling.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/1996/10/08/96-25811/oral-dosage-form-new-animal-drugs-oxytetracycline-hydrochloride-soluble-powder)
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