![]() This is the date the product will no longer be available on the market. This is the date that the labeler indicates was the start of its marketing of the drug product. The complete list of codes and translations can be found at under Structured Product Labeling Resources. Currently, only final marketed product categories are included. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. ![]() ![]() Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. Marketing Information:An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available. The translation of the Route Code submitted by the firm, indicating route of administration. Each ingredient name is the preferred term of the UNII code submitted. Therefore, all products in this file are considered unapproved. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found under Structured Product Labeling Resources.įDA does not review and approve unfinished products. The translation of the DosageForm Code submitted by the firm. Name of Company corresponding to the labeler code segment of the ProductNDC. This data element corresponds to the “Document Type” of the SPL submission for the listing.Īlso known as the generic name, this is usually the active ingredient(s) of the product. Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. It is the name of the product chosen by the labeler. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.Īlso known as the trade name. The labeler code and product code segments of the National Drug Code number, separated by a hyphen.
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