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REIMBURSEMENT POLICY CMS1500National Drug Code (NDC) Requirement Policy NumberAnnual 2017R6002A Approval Date12/14/2016Approved Reimbursement Policy Oversight CommitteeIMPORTANT NOTE ABOUT THIS REIMBURSEMENT
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National Drug Code (NDC) is a unique 10-digit, 3-segment number assigned to each medication listed under Section 510 of the U.S. Federal Food, Drug, and Cosmetic Act.
Manufacturers, repackagers, relabelers, and distributors of prescription drugs in the United States are required to file National Drug Code (NDC).
To fill out National Drug Code (NDC), you need to obtain a labeler code from the FDA, assign product codes for each drug product, and combine them with the package codes to create the unique 10-digit NDC.
The purpose of National Drug Code (NDC) is to identify and provide information about prescription drugs, including the manufacturer, product, and package size.
National Drug Code (NDC) must report the labeler code, product code, and package code for each drug product.
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