# Implantation or Injectable Dosage Form New Animal Drugs; Ceftiofur Hydrochloride
> **Food and Drug Administration** · Final rule. · Published 2008-08-06 · Effective 2008-08-06 · 73 FR 45611
## Document
- **Document number:** E8-18094
- **Category:** other
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 73 FR 45611
- **CFR reference:** 21 CFR 522
- **Publication date:** 2008-08-06
- **Effective date:** 2008-08-06
- **HHS docket:** Docket No. FDA-2008-N-0039
## 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 Pharmacia and Upjohn Co., a Division of Pfizer, Inc. The NADA provides for the veterinary prescription use of a ceftiofur hydrochloride injectable suspension for treatment of various bacterial infections in swine and cattle.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2008/08/06/E8-18094/implantation-or-injectable-dosage-form-new-animal-drugs-ceftiofur-hydrochloride)
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