# Oral Dosage Form New Animal Drugs; Oxytetracycline Hydrochloride Soluble Powder
> **Food and Drug Administration** · Final rule. · Published 1998-08-19 · Effective 1998-08-19 · 63 FR 44383
## Document
- **Document number:** 98-22266
- **Category:** other
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 63 FR 44383
- **CFR reference:** 21 CFR 520
- **Publication date:** 1998-08-19
- **Effective date:** 1998-08-19
## 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 provides for added package sizes of oxytetracycline hydrochloride (OTC HCI) soluble powder to be used in the drinking water of poultry for control of specific diseases, in the drinking water of cattle, swine, and sheep for control and treatment of specific diseases, and for control of specific diseases of bees.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/1998/08/19/98-22266/oral-dosage-form-new-animal-drugs-oxytetracycline-hydrochloride-soluble-powder)
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