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  4. NDC Product Code: 13267-123 Fludeoxyglucose F18

NDC 13267-123 Fludeoxyglucose F18

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 13267-123?
  4. Fludeoxyglucose F18 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:
13267-123
Proprietary Name:
Fludeoxyglucose F18
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
The Feinstein Institute For Medical Research
Labeler Code:
13267
Product Label ID:
96398ed5-ffb9-4ed4-92c1-6a9535864475
Start Marketing Date: [9]
08-19-2005
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 13267-123?

The NDC code 13267-123 is assigned by the FDA to the product Fludeoxyglucose F18 which is product labeled by The Feinstein Institute For Medical Research. The product's dosage form is . The product is distributed in a single package with assigned NDC code 13267-123-23 17 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 F18?

Fludeoxyglucose F18 Injection is indicated for positron emission tomography (PET) imaging in the following settings:

Which are Fludeoxyglucose F18 UNII Codes?

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

* Please review the disclaimer below.

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".