NDC Package 66715-6424-1 Mucinex Dm, Travel Basix

Guaifenesin And Dextromethorphan Hydrobromide Tablet, Extended Release 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:
66715-6424-1
Package Description:
1 POUCH in 1 CARTON / 2 TABLET, EXTENDED RELEASE in 1 POUCH
Product Code:
Proprietary Name:
Mucinex Dm, Travel Basix
Non-Proprietary Name:
Guaifenesin And Dextromethorphan Hydrobromide
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 or 2 tablets every 12 hours; not more than 4 tablets in 24 hourschildren under 12 years of age: do not use
11-Digit NDC Billing Format:
66715642401
NDC to RxNorm Crosswalk:
  • RxCUI: 1298324 - guaiFENesin 600 MG / dextromethorphan HBr 30 MG 12HR Extended Release Oral Tablet
  • RxCUI: 1298324 - 12 HR dextromethorphan hydrobromide 30 MG / guaifenesin 600 MG Extended Release Oral Tablet
  • RxCUI: 1298324 - dextromethorphan hydrobromide 30 MG / guaifenesin 600 MG 12 HR Extended Release Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Lil' Drug Store Products, Inc.
    Dosage Form:
    Tablet, Extended Release - A solid dosage form containing a drug which allows at least a reduction in dosing frequency as compared to that drug presented in conventional dosage form.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    NDA021620
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    11-29-2022
    Listing Expiration Date:
    12-31-2024
    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 66715-6424-1?

    The NDC Packaged Code 66715-6424-1 is assigned to a package of 1 pouch in 1 carton / 2 tablet, extended release in 1 pouch of Mucinex Dm, Travel Basix, a human over the counter drug labeled by Lil' Drug Store Products, Inc.. The product's dosage form is tablet, extended release and is administered via oral form.

    Is NDC 66715-6424 included in the NDC Directory?

    Yes, Mucinex Dm, Travel Basix with product code 66715-6424 is active and included in the NDC Directory. The product was first marketed by Lil' Drug Store Products, Inc. on November 29, 2022 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 66715-6424-1?

    The 11-digit format is 66715642401. 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
    5-4-166715-6424-15-4-266715-6424-01