NDC Package 63824-041-71 Mucinex D Maximum Strength

Guaifenesin And Pseudoephedrine Hydrochloride 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:
63824-041-71
Package Description:
24 POUCH in 1 CARTON / 1 TABLET, EXTENDED RELEASE in 1 POUCH
Product Code:
Proprietary Name:
Mucinex D Maximum Strength
Non-Proprietary Name:
Guaifenesin And Pseudoephedrine Hydrochloride
Substance Name:
Guaifenesin; Pseudoephedrine Hydrochloride
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:
63824004171
NDC to RxNorm Crosswalk:
  • RxCUI: 1244675 - guaiFENesin 1200 MG / pseudoephedrine HCl 120 MG 12HR Extended Release Oral Tablet
  • RxCUI: 1244675 - 12 HR guaifenesin 1200 MG / pseudoephedrine hydrochloride 120 MG Extended Release Oral Tablet
Product Type:
Human Otc Drug
Labeler Name:
Rb Health (us) Llc
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:
NDA021585
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
06-26-2012
Listing Expiration Date:
12-31-2026
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
63824-041-121 BLISTER PACK in 1 CARTON / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
63824-041-242 BLISTER PACK in 1 CARTON / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
63824-041-363 BLISTER PACK in 1 CARTON / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 63824-041-71?

The NDC Packaged Code 63824-041-71 is assigned to a package of 24 pouch in 1 carton / 1 tablet, extended release in 1 pouch of Mucinex D Maximum Strength, a human over the counter drug labeled by Rb Health (us) Llc. The product's dosage form is tablet, extended release and is administered via oral form.

Is NDC 63824-041 included in the NDC Directory?

Yes, Mucinex D Maximum Strength with product code 63824-041 is active and included in the NDC Directory. The product was first marketed by Rb Health (us) Llc on June 26, 2012 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 63824-041-71?

The 11-digit format is 63824004171. 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
5-3-263824-041-715-4-263824-0041-71