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  4. NDC Product Code: 24468-001 Fludeoxyglucose F-18

NDC 24468-001 Fludeoxyglucose F-18

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 24468-001?
  4. Fludeoxyglucose F-18 Uses
  5. Active Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
24468-001
Proprietary Name:
Fludeoxyglucose F-18
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
University Of North Dakota
Labeler Code:
24468
Product Label ID:
0eb82924-1ce4-680e-e054-00144ff88e88
Start Marketing Date: [9]
09-14-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 24468-001-10

Package Description: 10 mL in 1 VIAL, GLASS

Product Details

What is NDC 24468-001?

The NDC code 24468-001 is assigned by the FDA to the product Fludeoxyglucose F-18 which is product labeled by University Of North Dakota. The product's dosage form is . The product is distributed in a single package with assigned NDC code 24468-001-10 10 ml in 1 vial, glass . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Fludeoxyglucose F-18?

Fludeoxyglucose F 18 Injection,USP is indicated in PET (positron emission tomography) for:1. Identification of regions of abnormal glucose metabolism associated with foci of epileptic seizures.2. Assessment of abnormal glucose metabolism to assist in the evaluation of malignancy in patients with known or suspected abnormalities found by other testing modalities, or in patients with an existing diagnosis of cancer.3. Assessment of patients with coronary artery disease and left ventricular dysfunction, when used together with myocardial perfusion imaging, for the identification of left ventricular myocardium with residual glucose metabolism and reversible loss of systolic function.Fludeoxyglucose F 18 Injection, USP is not indicated for distinguishing epileptogenic foci from brain tumors or other brain lesions which may cause seizures.

Which are Fludeoxyglucose F-18 UNII Codes?

The UNII codes for the active ingredients in this product are:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".