# Implantation or Injectable Dosage Form New Animal Drugs; Flunixin
> **Food and Drug Administration** · Final rule. · Published 2009-02-12 · Effective 2009-02-12 · 74 FR 6993
## Document
- **Document number:** E9-2941
- **Category:** other
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 74 FR 6993
- **CFR reference:** 21 CFR 522
- **Publication date:** 2009-02-12
- **Effective date:** 2009-02-12
- **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 supplemental abbreviated new animal drug application (ANADA) filed by Cross Vetpharm Group Ltd. The supplemental ANADA provides for the veterinary prescription use of flunixin meglumine solution by intravenous injection in dairy cattle for control of pyrexia associated with acute bovine mastitis.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2009/02/12/E9-2941/implantation-or-injectable-dosage-form-new-animal-drugs-flunixin)
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