1. Home
  2. Labeler Index
  3. Yyba Corp
  4. 73581-405
  5. NDC Package Code: 73581-405-98 Mucus Relief - Dm Maximum Strength

NDC Package 73581-405-98 Mucus Relief - Dm Maximum Strength

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 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:
73581-405-98
Package Description:
98 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product Code:
73581-405
Proprietary Name:
Mucus Relief - Dm Maximum Strength
Usage Information:
• do not crush, chew, or break tablet • take with a full glass of water • this product can be administered without regard for timing of meals • adults and children 12 years and older: 1 tablet every 12 hours; not more than 2 tablets in 24 hours children under 12 years of age: do not use
11-Digit NDC Billing Format:
73581040598
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
Labeler Name:
Yyba Corp
Sample Package:
No
FDA Application Number:
ANDA214781
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
04-01-2025
Listing Expiration Date:
12-31-2026
Exclude Flag:
I
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 73581-405-98?

The NDC Packaged Code 73581-405-98 is assigned to a package of 98 tablet, extended release in 1 blister pack of Mucus Relief - Dm Maximum Strength, labeled by Yyba Corp. The product's dosage form is and is administered via form.

Is NDC 73581-405 included in the NDC Directory?

No, Mucus Relief - Dm Maximum Strength with product code 73581-405 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Yyba Corp on April 01, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 73581-405-98?

The 11-digit format is 73581040598. 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
5-3-273581-405-985-4-273581-0405-98