NDC Package 68016-550-50 Mucus Relief Dm

Dextromethorphan Hbr And Guaifenesin Tablet, Film Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Package Information

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:
68016-550-50
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Mucus Relief Dm
Non-Proprietary Name:
Dextromethorphan Hbr And Guaifenesin
Substance Name:
Dextromethorphan Hydrobromide; Guaifenesin
Usage Information:
Take with a full glass of wateradults and children 12 years and over: 1 tablet every 4 hours. Do not take more than 6 tablets in 24 hours.children under 12 years: do not use
11-Digit NDC Billing Format:
68016055050
NDC to RxNorm Crosswalk:
  • RxCUI: 1147685 - dextromethorphan HBr 20 MG / guaiFENesin 400 MG Oral Tablet
  • RxCUI: 1147685 - dextromethorphan hydrobromide 20 MG / guaifenesin 400 MG Oral Tablet
  • RxCUI: 1147685 - guaifenesin 400 MG / dextromethorphan HBr 20 MG Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Chain Drug Consortium
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    M012
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    01-12-2023
    Listing Expiration Date:
    12-31-2025
    Exclude Flag:
    N
    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.

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    Frequently Asked Questions

    What is NDC 68016-550-50?

    The NDC Packaged Code 68016-550-50 is assigned to a package of 1 bottle, plastic in 1 carton / 50 tablet, film coated in 1 bottle, plastic of Mucus Relief Dm, a human over the counter drug labeled by Chain Drug Consortium. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 68016-550 included in the NDC Directory?

    Yes, Mucus Relief Dm with product code 68016-550 is active and included in the NDC Directory. The product was first marketed by Chain Drug Consortium on January 12, 2023 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 68016-550-50?

    The 11-digit format is 68016055050. 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 5-3-2 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
    5-3-268016-550-505-4-268016-0550-50