NDC Package 11822-7329-2 Mucus Relief Maximum Strength

View Billable Units, 11-Digit Format, RxNorm

Package Information
Other Packages
Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:

11822-7329-2

Package Description:

14 BLISTER PACK in 1 CARTON / 1 TABLET in 1 BLISTER PACK

Product Code:

11822-7329

Proprietary Name:

Mucus Relief Maximum Strength

Usage Information:

Do not crush, chew, or break tablettake with a full glass of waterthis product can be administered without regard for the timing of meals adults and children 12 years of age and over: 1 tablet every 12 hours. Do not exceed 2 tablets in 24 hours.children under 12 years of age: do not use

11-Digit NDC Billing Format:

11822732902

NDC to RxNorm Crosswalk:

RxCUI: 310621 - guaiFENesin 1200 MG 12HR Extended Release Oral Tablet
RxCUI: 310621 - 12 HR guaifenesin 1200 MG Extended Release Oral Tablet
RxCUI: 310621 - guaifenesin 1200 MG 12 HR Extended Release Oral Tablet

Labeler Name:

Rite Aid Corporation

Sample Package:

FDA Application Number:

ANDA207342

Marketing Category:

ANDA - A product marketed under an approved Abbreviated New Drug Application.

Start Marketing Date:

01-31-2020

Listing Expiration Date:

12-31-2024

Exclude Flag:

Code Structure:

11822 - Rite Aid Corporation
- 11822-7329 - Mucus Relief
  - 11822-7329-2 - 14 BLISTER PACK in 1 CARTON / 1 TABLET in 1 BLISTER PACK

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 disclaimer below.

Other Product Packages

The following packages are also available for this product:

NDC Package Code	Package Description
11822-7329-8	28 BLISTER PACK in 1 CARTON / 1 TABLET in 1 BLISTER PACK

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 11822-7329-2?

The NDC Packaged Code 11822-7329-2 is assigned to a package of 14 blister pack in 1 carton / 1 tablet in 1 blister pack of Mucus Relief Maximum Strength, labeled by Rite Aid Corporation. The product's dosage form is and is administered via form.

Is NDC 11822-7329 included in the NDC Directory?

No, Mucus Relief Maximum Strength with product code 11822-7329 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Rite Aid Corporation on January 31, 2020 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 11822-7329-2?

The 11-digit format is 11822732902. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-4-1	11822-7329-2	5-4-2	11822-7329-02

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