NDC Package 55154-5783-5 Guaifenesin Dm

Guaifenesin And Dextromethorphan Syrup 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:
55154-5783-5
Package Description:
5 CUP, UNIT-DOSE in 1 BAG / 10 mL in 1 CUP, UNIT-DOSE
Product Code:
Proprietary Name:
Guaifenesin Dm
Non-Proprietary Name:
Guaifenesin And Dextromethorphan
Substance Name:
Dextromethorphan; Guaifenesin
Usage Information:
This product is used as Non-Narcotic, Alcohol Free Expectorant/Cough Suppressant . •helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive•temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold
11-Digit NDC Billing Format:
55154578305
NDC to RxNorm Crosswalk:
  • RxCUI: 996520 - dextromethorphan HBr 20 MG / guaiFENesin 200 MG in 10 mL Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 2 MG/ML / guaifenesin 20 MG/ML Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 10 MG / guaifenesin 100 MG per 5 ML Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 15 MG / guaifenesin 150 MG per 7.5 ML Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 20 MG / guaifenesin 200 MG per 10 ML Oral Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Cardinal Health 107, Llc
    Dosage Form:
    Syrup - An oral solution containing high concentrations of sucrose or other sugars; the term has also been used to include any other liquid dosage form prepared in a sweet and viscid vehicle, including oral suspensions.
    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:
    07-01-1992
    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 55154-5783-5?

    The NDC Packaged Code 55154-5783-5 is assigned to a package of 5 cup, unit-dose in 1 bag / 10 ml in 1 cup, unit-dose of Guaifenesin Dm, a human over the counter drug labeled by Cardinal Health 107, Llc. The product's dosage form is syrup and is administered via oral form.

    Is NDC 55154-5783 included in the NDC Directory?

    Yes, Guaifenesin Dm with product code 55154-5783 is active and included in the NDC Directory. The product was first marketed by Cardinal Health 107, Llc on July 01, 1992 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 55154-5783-5?

    The 11-digit format is 55154578305. 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
    5-4-155154-5783-55-4-255154-5783-05