Pro-den Rx
NDC Package 59883-166-16
Package Information
Pro-den Rx is a . Marketed by Den-mat Holdings, Llc, this product is identified by NDC 59883-166.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 59883 - Den-mat Holdings, Llc
- 59883-166 - Pro-den Rx
- 59883-166-16 - 473 mL in 1 TUBE
- 59883-166 - Pro-den Rx
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 59883-166-16 identifies a specific commercial package of 473 ml in 1 tube of Pro-den Rx, labeled by Den-mat Holdings, Llc. 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 Den-mat Holdings, Llc on November 21, 2008. The current certification is valid through December 31, 2014.
How is this Den-mat Holdings, Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 59883016616. 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.