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National Drug Code Directory
The Drug Listing Act of 1972 requires registered drug establishments to provide the Food and Drug Administration (FDA) with a current list of all drugs manufactured, prepared, propagated, compounded, or processed by it for commercial distribution. (See Section 510 of the Federal Food, Drug, and Cosmetic Act (Act) (21 U.S.C. � 360)). Drug products are identified and reported using a unique, three-segment number, called the National Drug Code (NDC), which serves as a universal product identifier for drugs. FDA publishes the listed NDC numbers and the information submitted as part of the listing information in the NDC Directory which is updated daily.
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건강보험심사평가원 약가마스터 의약품주성분
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의약품 주성분(일반명) 현황에 대한 데이터셋 입니다. / 의약품주성분 코드, 성분명, 제형구분, 투여, 함량, 단위 등 정보를 제공합니다.
보건복지부 국립춘천병원 의약품목록
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보건복지부 국립춘천병원 의약품 목록 데이터로, 약품코드, 약품영문명, 약품한글명, 구분의 항목으로 구성되어있습니다.
식품의약품안전처 원료의약품등록(DMF)현황
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식품의약품안전처에서 관리하는 의약품(허가,행정,성분 등)의 관련 정보 조회
FDA Drug Label Data
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This file contains the data elements used for searching the FDA Online Data Repository including proprietary name, active ingredients, marketing application number or regulatory citation, National Drug Code, and company name.
Code of Federal Regulations Title 21
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This database contains the most recent revision from the Government Printing Office (GPO) of the Code of Federal Regulations (CFR) Title 21 - Food and Drugs.
Drugs to be Discontinued
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Companies are required under Section 506C of the Federal Food, Drug, and Cosmetic Act (FD&C Act) (as amended by the Food and Drug Administration Safety and Innovation Act) to notify FDA of a permanent discontinuance of certain drug products, six months in advance, or if that is not possible, as soon as practicable. These drugs include those that are life-supporting, life-sustaining or for use in the prevention or treatment of a debilitating disease or condition, including any such drug used in emergency medical care or during surgery). The discontinuations provided below reflect information received from manufacturers, and are for informational purposes only.
식품의약품안전처 분류별 마약류취급자 정보
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마약류취급자 연도, 분류, 건수정보를 제공
FDA Notices of Judgment Collection, 1908-1966
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A digital archive of the published federal notices of judgment (a summary of the final outcome of a court case) for manufacturers and products prosecuted under authority of the 1906 Pure Food and Drug Act (https://fdanj.nlm.nih.gov/)
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