Food and Drug Administration/FDA 〈美〉食品及药品管理署 美国卫生及公共服务部〔Department of Health and Human Services〕的一个部门，负责为食品、药品、化妆品及其他作为消费品的家居用品设定安全及质量标准。其基本职能包括研究、检查和批准药物的制造与销售，并负责实施《食品、药品及化妆品法》〔Food, Drug and Cosmetic Act〕。 (→Food, Drug and Cosmetic Act)
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Food and Drug Administration. A division of the U.S. Public Health Service in the Department of Health and Human Services responsible for ensuring that food is safe, pure, and wholesome; that human and animal drugs, biological products, and medical devices are safe and effective; and that certain other products, such as electronic products that emit
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The first drug that contains a particular active ingredient that is approved by the FDA for a specified use.
Orange Book. Patents. A list of patents on drugs or drug products for which generic-drug applications may be submitted to the Food and Drug Administration. • The expiration dates of the patents are also listed. An applicant may submit a generic-drug application at any time, but the applicant must either accept deferral of FDA approval