![]() ![]() Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. NDA - A product marketed under an approved New Drug Application. This field Indicates whether this package is a sample packaging or not. Intravenous - Administration within or into a vein or veins.Kit - A packaged collection of related material. ![]() This data element matches the “Document Type” field of the Structured Product Listing.Īdvanced Accelerator Applications Usa, Inc Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. Human Prescription Drug What kind of product is this? The leading zeros must be added to the appropriate segment to create a 5-4-2 configuration.ĮA - Billing unit of "each" is used when the product is dispensed in discreet units. Netspot fda code#If the NDC Package code is less than 11 digits the code must be padded with leading zeros. The generic name usually includes the active ingredient(s) of the product.įor insurance billing purposes the Centers for Medicare & Medicaid Services (CMS) created an 11 digit NDC derivative identifier. The non-proprietary name is sometimes called the generic name. The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.Ħ8ga-dotatate What is the Non-Proprietary Name? Field Nameġ KIT in 1 KIT * 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE The product's dosage form is kit and is administered via intravenous form. The NDC Code 69488-001-40 is assigned to a package of 1 kit in 1 kit * 1 injection, powder, lyophilized, for solution in 1 vial, single-dose of Netspot, a human prescription drug labeled by Advanced Accelerator Applications Usa, Inc. ![]()
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