# Implantation or Injectable Dosage Form New Animal Drugs; Tulathromycin
> **Food and Drug Administration** · Final rule. · Published 2005-07-12 · Effective 2005-07-12 · 70 FR 39918
## Document
- **Document number:** 05-13586
- **Category:** other
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 70 FR 39918
- **CFR reference:** 21 CFR 522
- **Publication date:** 2005-07-12
- **Effective date:** 2005-07-12
## Abstract

The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of a new animal drug application (NADA) filed by Pfizer, Inc. The NADA provides for the veterinary prescription use of tulathromycin solution in cattle and in swine, by injection, for the management of respiratory disease. FDA is also amending the regulations to add the acceptable daily intake for total residues of tulathromycin and tolerances for residues of tulathromycin in edible tissues of cattle and swine.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2005/07/12/05-13586/implantation-or-injectable-dosage-form-new-animal-drugs-tulathromycin)
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