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  5. NDC Package Code: 66424-565-16 Sda Laboratories Tussin Dm

NDC Package 66424-565-16 Sda Laboratories Tussin Dm

Dextromethorphan Hbr,Guaifenesin Liquid Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
66424-565-16
Package Description:
473 mL in 1 BOTTLE
Product Code:
66424-565
Proprietary Name:
Sda Laboratories Tussin Dm
Non-Proprietary Name:
Dextromethorphan Hbr, Guaifenesin
Substance Name:
Dextromethorphan Hydrobromide; Guaifenesin
Usage Information:
Usestemporarilyrelievescoughduetominorthroatand bronchial irritationhelps loosen phlegm (mucus)helps thin bronchial secretions to make coughs more productive
11-Digit NDC Billing Format:
66424056516
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:
Sda Laboratories, Inc.
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
M012
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
12-01-2024
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 66424-565-16?

The NDC Packaged Code 66424-565-16 is assigned to a package of 473 ml in 1 bottle of Sda Laboratories Tussin Dm, a human over the counter drug labeled by Sda Laboratories, Inc.. The product's dosage form is liquid and is administered via oral form.

Is NDC 66424-565 included in the NDC Directory?

Yes, Sda Laboratories Tussin Dm with product code 66424-565 is active and included in the NDC Directory. The product was first marketed by Sda Laboratories, Inc. on December 01, 2024 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 66424-565-16?

The 11-digit format is 66424056516. 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
5-3-266424-565-165-4-266424-0565-16