Sodium Fluoride F 18 Injection
NDC Package 67939-020-10

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Sodium Fluoride F 18 injection is uSP is indicated for diagnostic positron emission tomography (PET) imaging of bone to define areas of altered osteogenic activity. This formulation utilizes a injection delivery system. Marketed by The University Of Utah Dba Cyclotron Radiochemistry Lab Huntsman Cancer Institute, this product is identified by NDC 67939-020 and is authorized under FDA application ANDA204497.

Identification & Billing

NDC Package Code
67939-020-10
Package Description
10 mL in 1 VIAL, MULTI-DOSE
Product Code
67939-020
11-Digit Billing Format
67939002010

Clinical Specifications

Proprietary Name
Sodium Fluoride F 18
Non-Proprietary Name
Sodium Fluoride F 18
Substance Name
Sodium Fluoride F-18
Dosage Form
Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
Administration Route
Intravenous - Administration within or into a vein or veins.
Active Ingredient(s)
SODIUM FLUORIDE F-18 200 mCi/mL
Pharmacologic Class
Usage Information
Sodium Fluoride F 18 Injection, USP is indicated for diagnostic positron emission tomography (PET) imaging of bone to define areas of altered osteogenic activity.

Regulatory & Marketing

Labeler Name
The University Of Utah Dba Cyclotron Radiochemistry Lab Huntsman Cancer Institute
Product Type
Human Prescription Drug
FDA Application #
ANDA204497
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
07-11-2012
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 67939-020-10 identifies a specific commercial package of 10 ml in 1 vial, multi-dose of Sodium Fluoride F 18, a human prescription drug labeled by The University Of Utah Dba Cyclotron Radiochemistry Lab Huntsman Cancer Institute. This injection is formulated for intravenous use and contains sodium fluoride f-18 as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by The University Of Utah Dba Cyclotron Radiochemistry Lab Huntsman Cancer Institute on July 11, 2012. The current certification is valid through December 31, 2026.

How is this The University Of Utah Dba Cyclotron Radiochemistry Lab Huntsman Cancer Institute product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 67939002010. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
67939-020-10
11-Digit CMS (5-4-2)
67939-0020-10

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.