# Animal Drug Availability Act; Medicated Feed Mill Licenses
> **Food and Drug Administration** · Final rule. · Published 1999-11-19 · Effective 1999-12-20 · 64 FR 63195
## Document
- **Document number:** 99-29856
- **Category:** hospital-facility
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 64 FR 63195
- **CFR reference:** 21 CFR 207
- **Publication date:** 1999-11-19
- **Effective date:** 1999-12-20
- **HHS docket:** Docket No. 97N-0276
## Abstract

The Food and Drug Administration (FDA) is publishing a final rule amending the new animal drug regulations to implement the medicated feed mill licensing requirements of the Animal Drug Availability Act of 1996 (ADAA). The ADAA amended the Federal Food, Drug, and Cosmetic Act (the act) to require that each facility that manufactures feeds containing approved new animal drugs possess a medicated feed mill license for the facility, rather than a separate medicated feed application (MFA) for each medicated feed manufactured by the facility, as previously required by the act. The final rule implements the feed mill licensing provisions of the ADAA.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/1999/11/19/99-29856/animal-drug-availability-act-medicated-feed-mill-licenses)
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