Allopurinol 5544

Name of Company corresponding to the labeler allopurinol 5544 segment of the ProductNDC. Indicates the type of product, such as Human Prescription Drug or Human OTC Drug.

The complete list of codes and translations can be found at www. Also known as the trade name. It is the name of the product chosen by the labeler. Although many companies follow certain naming conventions for suffices, there is no recognized standard. Drug for Further Processing, Bulk for Human Drug Compounding, and Bulk for Animal Drug Compounding.

FDA does not review and approve unfinished products. Therefore, all products having “unfinished” status are considered unapproved. This is the assigned DEA Schedule number as reported by the labeler. Values are CI, CII, CIII, CIV, and CV. The labeler code, product code, and package code segments of the National Drug Code number, separated by hyphens. Asterisks are no longer used or included within the product and package code segments to indicate certain configurations of the NDC. A description of the size and type of packaging in sentence form.

Multilevel packages will have the descriptions concatenated together. Defines whether given package serves sample purposes. NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. This is the date that the labeler indicates was the start of its marketing of the drug package.

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