National drug code directory
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National drug code directory

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Published by U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration in Rockville, Md .
Written in English

Subjects:

  • Information storage and retrieval systems -- Code numbers.,
  • Drugs.,
  • Catalogs, Drug -- United States.,
  • Drugs -- Nomenclature -- nomenclature.

Book details:

Edition Notes

Includes alphabetical indexes and numeric indexes.

Other titlesDrug code directory.
Statement[prepared by] Product Information Management Branch, Center for Drug Evaluation and Research.
GenreNomenclature
ContributionsCenter for Drug Evaluation and Research. Drug Registration & Listing System.
The Physical Object
Pagination2 v. ;
ID Numbers
Open LibraryOL22205928M

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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.   Unlike these five DKBs, the FDA National Drug Code directory currently does not include a clinical drug coding system, and is not directly comparable to the other five. We included the National Drug Code directory (obtained from the FDA website 8) in some of the analyses, in order to assess its coverage of “NDCs” in common by: The contents of the National Drug Codes List website are provided for educational purposes only and are not intended in any way as medical advice, medical diagnosis or treatment. Reliance on any information provided by the National Drug Codes List website or other . NDC Codes - National Drug Codes. The Drug Listing Act of 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.

Search NDC. What are the NDC Number and the National Drug Code Directory? Section of the Federal Food, Drug and Cosmetic Act (Act), 21 U.S.C. §, requires a registered drug establishments. The National Drug Code (NDC) is a unique product identifier used in the United States for drugs intended for human use. The Drug Listing Act of 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.   National Drug Code Directory Metadata Updated: Febru The Drug Listing Act of 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 by: 7. Medscape Drug Reference Search. MedWatch. Micromedex (Includes: Diseasedex, Drugdex, Indentidex, IV Index, Martindale, Poisondex, Red Book, Reprorisk) National drug code directory. National Center for Complementary and Alternative Medicine. Natural Medicines Comprehensive Database. NIDA Archive. Orange Book: Approved Drug Products with.

National drug code directory, October Prepared by Science information facility, Food and drug administration / Etats Unis. Department Health, education and welfare. Each listed drug product is assigned a unique digit, 3-segment number †. This number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. A labeler is any firm that manufactures (including repackers or relabelers), or distributes (under its own name) the drug.   The National Drug Code (NDC) number is a universal product identifier for drugs used in the United States. The Center for Medicare & Medicaid Services (CMS) has required NDC numbers to be reported when submitting claims for drugs and vaccines for more than 10 : George Blake. Title National drug code directory (Online) National drug code directory / U.S. Food and Drug Administration, Center for Drug Evaluation and Research. Format Online Resource Book Published [Rockville, Md.]: U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Drug Evaluation and Research, Division of Data Management and Services.