NDC Package 73581-404-05 Mucus Relief - Dm Maximum Strength

Guaifenesin,Dextromethorphan Hbr Tablet 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:
73581-404-05
Package Description:
50 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Mucus Relief - Dm Maximum Strength
Non-Proprietary Name:
Guaifenesin, Dextromethorphan Hbr
Substance Name:
Dextromethorphan Hydrobromide; Guaifenesin
Usage Information:
Do not crush, chew, or break tablettake with a full glass of waterthis product can be administered without regard for timing of mealsadults and children 12 years and older: 1 tablet every 12 hours; not more than 2 tablets in 24 hourschildren under 12 years of age: do not use
11-Digit NDC Billing Format:
73581040405
NDC to RxNorm Crosswalk:
  • RxCUI: 1099074 - guaiFENesin 1200 MG / dextromethorphan HBr 60 MG 12HR Extended Release Oral Tablet
  • RxCUI: 1099074 - 12 HR dextromethorphan hydrobromide 60 MG / guaifenesin 1200 MG Extended Release Oral Tablet
  • RxCUI: 1099074 - dextromethorphan hydrobromide 60 MG / guaifenesin 1200 MG 12 HR Extended Release Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Yyba Corp
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    ANDA206941
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    05-25-2023
    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.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 73581-404-05?

    The NDC Packaged Code 73581-404-05 is assigned to a package of 50 tablet in 1 bottle of Mucus Relief - Dm Maximum Strength, a human over the counter drug labeled by Yyba Corp. The product's dosage form is tablet and is administered via oral form.

    Is NDC 73581-404 included in the NDC Directory?

    Yes, Mucus Relief - Dm Maximum Strength with product code 73581-404 is active and included in the NDC Directory. The product was first marketed by Yyba Corp on May 25, 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 73581-404-05?

    The 11-digit format is 73581040405. 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
    5-3-273581-404-055-4-273581-0404-05