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12 Ιουν 2024 · The NDC, or National Drug Code, is a unique 10-digit or 11-digit, 3-segment number, and a universal product identifier for human drugs in the United States. The 3 segments of the NDC identify: the labeler, the product, and the commercial package size.
28 Σεπ 2023 · Format of the National Drug Code. FDA/OC/OUDLC/DRLB. Julian Chun, PharmD, MBA, BCACP, RAC-drug Consumer Safety Officer September 28, 2023. Objectives. Define the National Drug Code (NDC)...
The NDC Directory contains information on active and certified finished and unfinished drugs submitted to FDA in structured product labeling (SPL) electronic listing files by labelers.
Format. The national drug code is a unique 10 or 11 digit, 3-segment numeric identifier assigned to each medication listed under Section 510 of the US Federal Food, Drug, and Cosmetic Act. The segments identify the labeler or vendor, product (within the scope of the labeler), and trade package (of this product).
What is National Drug Code (NDC)? A unique 10-digit, 3-segment number. Universal product identifier for drugs. Should not be assigned to non-drug products. Submission of NDC is required for...
(a) What is the NDC for a drug and what products must have unique NDCs? The NDC for a drug is a numeric code. Each finished drug product or unfinished drug subject to the listing requirements of this part must have a unique NDC to identify its labeler, product, and package size and type.
The Drug Listing Act of 1972 requires registered drug establishments to provide the Food and Drug Administration (FDA) with a current list of all drugs manufactured, prepared,...
