NDC 0407-0690-05 Omniscan

Gadodiamide

NDC Package Code 0407-0690-05

Field Name Field Value
NDC Code 0407-0690-05
Package Description 10 VIAL in 1 BOX > 5 mL in 1 VIAL
Proprietary Name Omniscan What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name Gadodiamide What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
11-Digit NDC Billing Format 00407069005 NDC Format for Billing
For insurance billing purposes the Centers for Medicare & Medicaid Services (CMS) created an 11 digit NDC derivative identifier. If the NDC Package code is less than 11 digits the code must be padded with leading zeros. The leading zeros must be added to the appropriate segment to create a 5-4-2 configuration.
Billing Unit ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
Product Type Human Prescription Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
Labeler Name Ge Healthcare Inc.
Dosage Form Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
Administration Route(s)
  • Intravenous - Administration within or into a vein or veins.
  • Intravenous - Administration within or into a vein or veins.
  • Intravenous - Administration within or into a vein or veins.
Active Ingredient(s)
  • GADODIAMIDE 287 mg/mL
  • GADODIAMIDE 287 mg/mL
  • GADODIAMIDE 287 mg/mL
Pharmacological Class(es)
  • Magnetic Resonance Contrast Activity - [MoA] (Mechanism of Action)
  • Paramagnetic Contrast Agent - [EPC] (Established Pharmacologic Class)
  • Magnetic Resonance Contrast Activity - [MoA] (Mechanism of Action)
  • Paramagnetic Contrast Agent - [EPC] (Established Pharmacologic Class)
  • Magnetic Resonance Contrast Activity - [MoA] (Mechanism of Action)
  • Paramagnetic Contrast Agent - [EPC] (Established Pharmacologic Class)
Sample Package No Sample Package?
This field Indicates whether this package is a sample packaging or not.
Marketing Category NDA - A product marketed under an approved New Drug Application. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
FDA Application Number NDA020123 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
Start Marketing Date 06-01-2010 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date 12-31-2019 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

The NDC Code 0407-0690-05 is assigned to Omniscan, a human prescription drug labeled by Ge Healthcare Inc.. The product's dosage form is injection and is administered via intravenous form.


Code Structure
  • 0407 - Ge Healthcare Inc.
    • 0407-0690 - Omniscan
      • 0407-0690-05 - 10 VIAL in 1 BOX

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

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NDC HCPCS Crosswalk

This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.

NDC 0407-0690-05 HCPCS crosswalk information with package details and bill units information.

NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
00407069005A9579Gad-base mr contrast nos,1ml1 ML510550

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Other Product Packages

The following packages are also available for Omniscan with product NDC 0407-0690.

NDC Package CodePackage Description
0407-0690-1010 VIAL in 1 BOX > 10 mL in 1 VIAL
0407-0690-1210 SYRINGE, PLASTIC in 1 BOX > 10 mL in 1 SYRINGE, PLASTIC
0407-0690-1510 VIAL in 1 BOX > 15 mL in 1 VIAL
0407-0690-1710 SYRINGE, PLASTIC in 1 BOX > 15 mL in 1 SYRINGE, PLASTIC
0407-0690-2010 VIAL in 1 BOX > 20 mL in 1 VIAL
0407-0690-2210 SYRINGE, PLASTIC in 1 BOX > 20 mL in 1 SYRINGE, PLASTIC
0407-0690-3010 VIAL in 1 BOX > 10 mL in 1 VIAL
0407-0690-4010 VIAL in 1 BOX > 15 mL in 1 VIAL
0407-0690-4210 SYRINGE in 1 BOX > 15 mL in 1 SYRINGE
0407-0690-4310 SYRINGE in 1 BOX > 20 mL in 1 SYRINGE
0407-0690-5010 VIAL in 1 BOX > 20 mL in 1 VIAL
0407-0690-7010 BOTTLE, PLASTIC in 1 BOX > 100 mL in 1 BOTTLE, PLASTIC

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