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EUROPEAN COMMISSION Brussels, 24.8.2020 COM(2020) 406 final ANNEXANNEX to the Proposal for a Council Decision on the position to be taken on behalf of the European Union within the Association Council
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Update of Form NDC refers to the process of submitting any changes or revisions to the Form NDC, which is used to report new drug codes for pharmaceutical products.
Manufacturers, repackagers, relabelers, and distributors of pharmaceutical products are required to file updates of Form NDC.
To fill out an update of Form NDC, the filer must provide the necessary information about the changes or revisions being made to the drug code, including the reason for the update.
The purpose of updating Form NDC is to ensure accurate and up-to-date information on pharmaceutical products, including new drug codes, is maintained in the database.
The information reported on an update of Form NDC may include changes to the drug code, product name, manufacturer information, labeling, packaging, or other relevant details.
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