An NDC number, or National Drug Code, is a unique identifier assigned to drugs and other healthcare products by the Food and Drug Administration (FDA) in the United States. The NDC number is a three-segment, numerical identifier that is used to identify a specific drug product and its packaging.
The first segment of the NDC number is a three-digit labeler code, which identifies the manufacturer or distributor of the drug product. The second segment is a four-digit product code, which identifies the specific drug product. The third segment is a two-digit package code, which identifies the type of packaging and quantity of the drug product.
NDC numbers are used in various ways in the pharmaceutical industry, they are used as a key element in prescription drugs and medical devices reporting systems, such as the FDA's Adverse Event Reporting System (FAERS) and the Vaccine Adverse Event Reporting System (VAERS). They also play a critical role in tracking and traceability systems, such as the Drug Supply Chain Security Act (DSCSA) which aims to improve the safety and security of the drug supply chain in the U.S.
In addition, NDC numbers are also used for reimbursement purposes, including billing and reimbursement for prescription drugs covered by government and private health insurance plans. This is used for the healthcare providers and insurance companies for identifying and processing claims for prescription drugs.
In summary, NDC number is a unique identifier assigned to drugs and other healthcare products by the Food and Drug Administration (FDA) in the United States. The NDC number is a three-segment, numerical identifier that is used to identify a specific drug product and its packaging. NDC numbers are widely used in the pharmaceutical industry, they are used as key element in reporting systems and tracking and traceability systems, they also used for reimbursement purposes.
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