Wellements Throat Pops
NDC Package 73328-001-10
Package Information
Wellements Throat Pops is a . Marketed by Wellements Llc, this product is identified by NDC 73328-001 and is authorized under FDA application part356.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 73328 - Wellements Llc
- 73328-001 - Wellements Throat Pops
- 73328-001-10 - 10 LOZENGE in 1 BOX
- 73328-001 - Wellements Throat Pops
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 73328-001-10 identifies a specific commercial package of 10 lozenge in 1 box of Wellements Throat Pops, labeled by Wellements 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 Wellements Llc on October 03, 2019. The current certification is valid through November 05, 2021.
How is this Wellements Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 73328000110. 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.