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HHS/FDA RIN: 0910-AF78 Publication ID: Fall 2006 
Title: Import Tolerances for Animal Drugs 
Abstract: FDA plans to publish a proposed rule related to the implementation of the import tolerances provision of the Animal Drug Availability Act of 1996 (ADAA). The ADAA authorizes FDA to establish drug residue tolerances (import tolerances) for imported food products of animal origin for drugs that are used in other countries, but that are unapproved new animal drugs in the United States. Food products of animal origin that are in compliance with the import tolerances will not be considered adulterated under the Federal Food, Drug, and Cosmetic Act (the Act) and may be imported into the United States. 
Agency: Department of Health and Human Services(HHS)  Priority: Substantive, Nonsignificant 
RIN Status: Previously published in the Unified Agenda Agenda Stage of Rulemaking: Proposed Rule Stage 
Major: No  Unfunded Mandates: No 
CFR Citation: Not Yet Determined (To search for a specific CFR, visit the Code of Federal Regulations.
Legal Authority: 21 USC 360b(a)(6); 21 USC 371 
Legal Deadline:  None
Timetable:
Action Date FR Cite
NPRM  03/00/2007   
Regulatory Flexibility Analysis Required: No  Government Levels Affected: None 
Small Entities Affected: No  Federalism: No 
Included in the Regulatory Plan: No 
Agency Contact:
George Kenneth Haibel
Veterinary Medical Officer
Department of Health and Human Services
Food and Drug Administration
Room 169 (MPN-4, HFV-6), 7519 Standish Place,
Rockville, MD 20855
Phone:240 276-9019
Fax:240 276-9101
Email: george.haibel@fda.hhs.gov

 
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