DEFINITIONS.

SEC. 2302. DEFINITIONS. Section 739 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 379j-11) is amended— (1) in paragraph (3), by striking “national drug code” and inserting “National Drug Code”; and (2) by amending paragraph (8)(I) to read as follows: “(I) The activities necessary for implementation of the United States and European Union Mutual Recognition Agreement for Pharmaceutical Good Manufacturing Practice Inspections, and the United States and United Kingdom Mutual Recognition Agreement Sectoral Annex for Pharmaceutical Good Manufacturing Practices, and other mutual recognition agreements, with respect to animal drug products subject to review, including implementation activities prior to and following product approval.” .