# Implantation or Injectable Dosage Form New Animal Drugs; Tulathromycin
> **Food and Drug Administration** · Final rule. · Published 2007-09-26 · Effective 2007-09-26 · 72 FR 54539
## Document
- **Document number:** E7-18983
- **Category:** other
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 72 FR 54539
- **CFR reference:** 21 CFR 522
- **Publication date:** 2007-09-26
- **Effective date:** 2007-09-26
## 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 the addition of a pathogen to the indication for use of tulathromycin, by injection, for the control of respiratory disease in high-risk cattle.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2007/09/26/E7-18983/implantation-or-injectable-dosage-form-new-animal-drugs-tulathromycin)
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