Technescan Hdp Injection, Powder, Lyophilized, For Solution
NDC Package 69945-091-20
Package Information
Technescan Hdp (technetium tc 99m oxidronate) injection is technescan HDP Tc 99m is a diagnostic skeletal imaging agent used to demonstrate areas of altered osteogenesis in adult and pediatric patients. This formulation utilizes a injection, powder, lyophilized, for solution delivery system. Marketed by Curium Us Llc, this product is identified by NDC 69945-091 and is authorized under FDA application NDA018321.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 69945 - Curium Us Llc
- 69945-091 - Technescan Hdp
- 69945-091-20 - 5 VIAL in 1 CELLO PACK / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (69945-091-01)
- 69945-091 - Technescan Hdp
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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Other Available Packages
The following commercial packages are registered under the same Product NDC (69945-091). Click a package code to view its specific billing and regulatory data.
* 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 69945-091-20 identifies a specific commercial package of 5 vial in 1 cello pack / 1 injection, powder, lyophilized, for solution in 1 vial (69945-091-01) of Technescan Hdp, a human prescription drug labeled by Curium Us Llc. This injection, powder, lyophilized, for solution is formulated for intravenous use and contains oxidronate disodium 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 Curium Us Llc on October 13, 2015. The current certification is valid through December 31, 2026.
How is this Curium Us Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 69945009120. 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:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.