Mucus Relief Dm
NDC Package 37808-812-66

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Mucus Relief Dm is •do not crush, chew, or break tablet•take with a full glass of water •this product can be administered without regard for timing of meals •adults and children 12 years and older: 1 tablet every 12 hours; not more than 2 tablets in 24 hours•children under 12 years of age: do not use. Marketed by H E B, this product is identified by NDC 37808-812 and is authorized under FDA application ANDA207602.

Identification & Billing

NDC Package Code
37808-812-66
Package Description
1 BOTTLE in 1 CARTON / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Code
37808-812
11-Digit Billing Format
37808081266

Clinical Specifications

Proprietary Name
Mucus Relief Dm
Dosage Form
-
Usage Information
•do not crush, chew, or break tablet•take with a full glass of water •this product can be administered without regard for timing of meals •adults and children 12 years and older: 1 tablet every 12 hours; not more than 2 tablets in 24 hours•children under 12 years of age: do not use

Regulatory & Marketing

Labeler Name
H E B
FDA Application #
ANDA207602
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
06-25-2018
End Marketing Date
09-30-2020
Listing Expiration
09-30-2020
Exclude Flag
D
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 37808-812-66 identifies a specific commercial package of 1 bottle in 1 carton / 14 tablet, extended release in 1 bottle of Mucus Relief Dm, labeled by H E B. 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 H E B on June 25, 2018. The current certification is valid through September 30, 2020.

How is this H E B product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 37808081266. 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)
37808-812-66
11-Digit CMS (5-4-2)
37808-0812-66

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