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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.

Source: OpenFDATest
FieldValue
Publisher
Modified
2013-11-14
Release Date
2013-11-14
Homepage URL
Identifier
2b7ec03d-67dc-4544-b1d6-b9aa02f693c6
License
License Not Specified
Data Dictionary
Contact Name
openFDA
Contact Email
Public Access Level
Public
Harvested from OpenFDATest
Harvest Source TitleOpenFDATest
Harvest Source URIhttps://open.fda.gov/data.json
Last Harvest PerformedThu, 01/10/2019 - 00:04