Ultra-technekow
NDC Package 0019-9883-03
Package Information
Ultra-technekow is a . Marketed by Mallinckrodt Inc., this product is identified by NDC 0019-9883 and is authorized under FDA application NDA017243.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 0019 - Mallinckrodt Inc.
- 0019-9883 - Ultra-technekow
- 0019-9883-03 - 1 INJECTION, SOLUTION in 1 CARTON
- 0019-9883 - Ultra-technekow
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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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 0019-9883-03 identifies a specific commercial package of 1 injection, solution in 1 carton of Ultra-technekow Dte, labeled by Mallinckrodt Inc.. This is formulated for use and contains as the active substance.
Is this product currently listed with the FDA?
This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Mallinckrodt Inc. on July 16, 1996. The current certification is valid through July 01, 2017.
How is this Mallinckrodt Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00019988303. 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 Labeler segment to maintain the 5-4-2 structure.