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  5. NDC Package Code: 70518-0466-0 Mucinex

NDC Package 70518-0466-0 Mucinex

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory .

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:
70518-0466-0
Package Description:
20 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Product Code:
70518-0466
Proprietary Name:
Mucinex
Usage Information:
This medication is used for the temporary relief of coughs caused by the common cold, bronchitis, and other breathing illnesses. This product is usually not used for ongoing cough from smoking or long-term breathing problems (such as chronic bronchitis, emphysema) unless directed by your doctor. Guaifenesin is an expectorant. It works by thinning and loosening mucus in the airways, clearing congestion, and making breathing easier. If you are self-treating with this medication, it is important to read the package instructions carefully before you start using this product to be sure it is right for you. (See also Precautions section.) Cough-and-cold products have not been shown to be safe or effective in children younger than 6 years. This product (sustained-release) is not recommended for use in children younger than 12 years unless specifically directed by the doctor. Ask your doctor or pharmacist for more details about using your product safely. These products do not cure or shorten the length of the common cold. To decrease the risk for side effects, carefully follow all dosage directions. Do not give other cough-and-cold medication that might contain the same or similar ingredients (see also Drug Interactions section). Ask the doctor or pharmacist about other ways to relieve cough and cold symptoms (such as drinking enough fluids, using a humidifier or saline nose drops/spray).
11-Digit NDC Billing Format:
70518046600
Labeler Name:
Remedyrepack Inc.
Sample Package:
No
FDA Application Number:
NDA021282
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
04-27-2017
End Marketing Date:
04-06-2020
Listing Expiration Date:
04-06-2020
Exclude Flag:
D
Code Structure:

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.

Frequently Asked Questions

What is NDC 70518-0466-0?

The NDC Packaged Code 70518-0466-0 is assigned to a package of 20 tablet, extended release in 1 bottle, plastic of Mucinex, labeled by Remedyrepack Inc.. The product's dosage form is and is administered via form.

Is NDC 70518-0466 included in the NDC Directory?

The product was first marketed by Remedyrepack Inc. on April 27, 2017 and its listing in the NDC Directory is set to expire on April 06, 2020 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 70518-0466-0?

The 11-digit format is 70518046600. 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 Format10-Digit Original Code11-Digit Format11-Digit Code
5-4-170518-0466-05-4-270518-0466-00