National Drug Code (NDC) definition

National Drug Code (NDC) means the identifying drug number maintained by the Food and Drug Administration (FDA). For purposes of the Agreement, the NDC number will be used including labeler code (which is assigned by the FDA and identifies the establishment), product code (which identifies the specified product or formulation), and package size code when reporting requested information.

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National Drug Code (NDC) means the identifying prescription drug product number that is listed with the Food and Drug Administration (FDA). For the purposes of this Agreement, unless otherwise specified, the NDC refers to the 11-digit (inclusive of 5 digit labeler code, 4 digit product code, and 2 digit package size code) NDC.

National Drug Code (NDC) means the three-segment code maintained by the federal Food and Drug Administration that includes a labeler code, a product code, and a package code for a drug product and that has been converted to an 11-digit format consisting of five digits in the first segment, four digits in the second segment, and two digits in the third segment. A three-segment code shall be considered converted to an 11-digit format when, as necessary, at least one “0” has been added to the front of each segment containing less than the specified number of digits such that each segment contains the specified number of digits.

Examples of National Drug Code (NDC) in a sentence

Requirements for pharmacy encounter claims are outlined in Section 8.5. The report will include information on the total number of units of each dosage form, strength and package size by National Drug Code (NDC) of each covered outpatient drug dispensed to Contractor members and such other data that the Secretary of CMS determines necessary for the State to access rebates.
Per 42 CFR 438.3(s)(2) and section 1927(b)(1)(A) of the Social Security Act, the report will include information on the total number of units of each dosage form, strength, and package size by National Drug Code (NDC) of each covered outpatient drug dispensed to Contractor members and such other data that the Secretary of CMS determines necessary for the State to access rebates.
Requirements for pharmacy encounter claims are outlined in Section 11.6. The report will include information on the total number of units of each dosage form, strength and package size by National Drug Code (NDC) of each covered outpatient drug dispensed to Contractor members and such other data that the Secretary of CMS determines necessary for the State to access rebates.
National Drug Code (NDC) – a unique 11-digit number which is a universal product identifier for human drugs.
The report will include information on the total number of units of each dosage form, strength and package size by National Drug Code (NDC) of each covered outpatient drug dispensed to Contractor members and such other data that the Secretary of CMS determines necessary for the State to access rebates.

More Definitions of National Drug Code (NDC)

National Drug Code (NDC) means the identifying prescription drug product number that is registered and listed with the Food and Drug Administration (FDA). Unless specified in this guidance, the NDC refers to either the 9 digit (inclusive of 5 digit labeler code and 4 digit product code) or 11 digit NDC (inclusive of 5 digit labeler code, 4 digit product code, and 2 digit package size code).

National Drug Code (NDC) means the eleven digit number the manufacturer or labeler assigns to a pharmaceuti- cal product and attaches to the product container at the time of packaging. The eleven-digit NDC is composed of a five- four-two grouping. The first five digits comprise the labeler code assigned to the manufacturer by the Federal Drug Administration (FDA). The second grouping of four digits is assigned by the manufacturer to describe the ingredients, dose form, and strength. The last grouping of two digits describes the package size.

National Drug Code (NDC) means the unique three-segment number used for identification and reporting as set forth in 21 CFR §207.33.

National Drug Code (NDC) means the eleven-digit number the manufacturer or labeler assigns to a pharmaceutical product and attaches to the product container at the time of packaging that identifies the product's manufacturer, dose form and strength, and package size.

National Drug Code (NDC). – means an 11-digit number that identifies a drug product. The first five digits represent the labeler code identifying the drug manufacturer; the next four digits identify the drug product; and the last two digits identify the package size.

National Drug Code (NDC) has the meaning given such term in 42 CFR § 423.2305. For

National Drug Code (NDC) means the unique, three- segment number, that identifies the labeler, product, and trade package size of human drugs.