# Oral Dosage Form New Animal Drugs; Cyclosporine
> **Food and Drug Administration** · Final rule. · Published 2011-12-20 · Effective 2011-12-20 · 76 FR 78815
## Document
- **Document number:** 2011-32526
- **Category:** other
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 76 FR 78815
- **CFR reference:** 21 CFR 520
- **Publication date:** 2011-12-20
- **Effective date:** 2011-12-20
- **HHS docket:** Docket No. FDA-2011-N-0003
## 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 Novartis Animal Health US, Inc. The NADA provides for the veterinary prescription use of cyclosporine oral solution, USP (MODIFIED) for the control of feline allergic dermatitis.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2011/12/20/2011-32526/oral-dosage-form-new-animal-drugs-cyclosporine)
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