# Oral Dosage Form New Animal Drugs; Phenylpropanolamine
> **Food and Drug Administration** · Final rule. · Published 2012-03-19 · Effective 2012-03-19 · 77 FR 15961
## Document
- **Document number:** 2012-6553
- **Category:** other
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 77 FR 15961
- **CFR reference:** 21 CFR 520
- **Publication date:** 2012-03-19
- **Effective date:** 2012-03-19
- **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 an original new animal drug application (NADA) filed by Pegasus Laboratories, Inc. The NADA provides for the veterinary prescription use of phenylpropanolamine hydrochloride chewable tablets for the control of urinary incontinence due to urethral sphincter hypotonus in dogs.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2012/03/19/2012-6553/oral-dosage-form-new-animal-drugs-phenylpropanolamine)
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