NDC definition

NDC means National Drug Code.
NDC means the “National Drug Code”, which is the eleven digit code registered by a company with the FDA with respect to a pharmaceutical product.

Examples of NDC in a sentence

  • MANUFACTURER DELAWARE DEPARTMENT OF HEALTH AND SOCIAL SERVICES By: Name: Xxxxxx Xxxxxx Title: DMMA Director Date: By: Name: Title: Date: Contracted Products Attachment Manufacturer NDC Product Description Tier Formula Contracted Rate Comments 1 Tiers The Tier represents the number of brand drugs that may be preferred in the Contracted Product PDL category.

  • Please contact the NDC on methods for downloading voucher information associated with your electronic payment.

  • If you are a creditor with access to the National Data Center you may prefer to download your voucher information from the NDC.

  • It is understood that the Pharmaceutical Manufacturer is liable for the payment of State Supplemental Rebates only for Covered Products (as identified by the 11-digit NDC code) distributed (directly or through the wholesale channel) to retail Pharmacies and dispensed to Medicaid Members.

  • NP Thyroid® (Thyroid Tablets, USP) (“NP Thyroid”), manufactured by or on behalf of Acella and marketed by Acella and/or any related entity, and all its ingredients, in all available dosage strengths and package sizes, as identified by all applicable NDC codes, 00000-000-00, 00000-000-00, 00000-000-00, 00000-000-00, and 00000-000-00.


More Definitions of NDC

NDC means “National Drug Code,” which is the eleven digit code registered by a company with the FDA with respect to a pharmaceutical product.
NDC means No Demand Certificate.
NDC means the National Drug Codes of the Food and Drug Administration.
NDC means the unique national drug code number that identifies a specific approved drug.
NDC means a unique 3-segment number that identifies the labeler/vendor, the product and the trade package size.
NDC means the unique, identifying number assigned to a drug product, including the labeler code, product code and package code, in connection with the drug listing requirements of Section 510(j) of the FD&C Act and applicable FDA rules and regulations.