Search for NDC (National Drug Code), Pack Style and Dailymed Label

Product Name Pack Description NDC Code Dailymed Label Pharmaceutical Class Labeler Name Marketing Start Date Marketing End Date
National Drug Code (NDC) Directory

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.

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. ยง 360)).

Reference

https://www.fda.gov/drugs/informationondrugs/ucm142438.htm

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