- The NDC Directory contains ONLY information on final marketed drugs submitted to FDA in SPL electronic listing files by labelers. (A labeler may be either a manufacturer, including a repackager or relabeler, or, for drugs subject to private labeling arrangements, the entity under whose own label or trade name the product will be distributed.) Inclusion of information in the NDC Directory does not indicate that FDA has verified the information provided. The content of each NDC Directory entry is the responsibility of the labeler submitting the SPL file.Assignment of an NDC number does not in any way denote FDA approval of the product. Any representation that creates an impression of official approval because of possession of an NDC number is misleading and constitutes misbranding. (21 CFR 207.39)
- Assignment of an NDC number does not in any way denote FDA approval of the product. Any representation that creates an impression of official approval because of possession of an NDC number is misleading and constitutes misbranding. (21 CFR 207.39)
- Neither inclusion in the NDC Directory nor possession of an NDC number is a determination that a product is a drug as defined by the FD&C Act, nor does either denote that a product is covered or eligible for reimbursement by Medicare, Medicaid or other payers. Assignment of NDC number to non-drug products is extremely prohibited.
- The NDC Directory does not contain all listed drugs. The new version includes the final marketed drugs which listing information were submitted electronically. It does not include animal drugs, blood products, or human drugs that are not in final marketed form, such as Active Pharmaceutical Ingredients (APIs), drugs for further processing, drugs manufactured exclusively for a private label distributor, or drugs that are marketed solely as part of a kit or combination product or inner layer of a multi-level packaged product not marketed individually.
- Only the OUTERMOST packages and dispensable inner layer packages, reported by firms as part of their product listing submission to the FDA, are included in the NDC Directory. This applies to co-packaged products listed as kits and multi-level packaged products.
The inner level of a multi level packaging or components of a kit will be included in the package description of the product to show the relationship between all layers and parts as reported by the listing firm.
If a product contained within a kit is approved/ authorized to be marketed separately, then a separate SPL file must be submitted.
If the inner level of a multi level packaging is a marketable/ dispensable layer, the NDCPackageCode assigned to it should be reported as a separate package code on the same listing SPL.
The relation between different levels of a multi level packaged product or components of a kit is still provided in the package description section. For any additional information, users can go to the FDA Online Label Repository page: http://labels.fda.gov/
ProductID is a concatenation of the NDCproduct code and SPL documentID. It is included to help prevent duplicate rows from appearing when joining the product and package files together. It has no regulatory value or significance.
Values = ‘E’, ‘U’, or ‘I’. This indicates whether the PACKAGE has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions (‘E’), or because the listing certification is expired due to lack of listing certification (‘U’), or because the listing data was inactivated by FDA (‘I’). The PACKAGE.XLS and PACKAGE.TXT files only contain listing records that are not flagged. The PACKAGES_EXCLUDED.XLS and PACKAGES_EXCLUDED.TXT file contains all listing records with an NDC_EXCLUDE_FLAG of ‘E’, ‘U’, and ‘I’.
This indicates if the package is to be distributed as a sample package. Values = ‘Y’ or ‘N’