National Drug Code Directory

Metadata Updated: February 26, 2019

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.

Access & Use Information

Public: This dataset is intended for public access and use. License: See this page for license information.

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Dates

Metadata Created Date June 19, 2015
Metadata Updated Date February 26, 2019

Metadata Source

Harvested from Healthdata.gov

Additional Metadata

Resource Type Dataset
Metadata Created Date June 19, 2015
Metadata Updated Date February 26, 2019
Publisher Department of Health & Human Services
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Maintainer
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Maintainer Email
Public Access Level public
Bureau Code 009:10
Metadata Context https://project-open-data.cio.gov/v1.1/schema/catalog.jsonld
Metadata Catalog ID https://healthdata.gov/data.json
Schema Version https://project-open-data.cio.gov/v1.1/schema
Catalog Describedby https://project-open-data.cio.gov/v1.1/schema/catalog.json
Harvest Object Id b28618cd-0f79-474b-acd3-bc9588a0b5ee
Harvest Source Id 15c538b5-31a0-474e-8ba5-c85ee421cb4d
Harvest Source Title Healthdata.gov
License https://opendatacommons.org/licenses/odbl/1.0/
Data Last Modified 2016-04-05
Program Code 009:002
Source Datajson Identifier True
Source Hash de47521ed776b6b38cd8b4f410fedd9c7d20fed4
Source Schema Version 1.1

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