Tussin Dm Cough And Chest Congestion Liquid
NDC Package 49580-0385-2

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Tussin Dm Cough And Chest Congestion (dextromethorphan hbr, guaifenesin) liquids is do not take more than 6 doses in any 24-hour periodmeasure only with the dosing cup provided. This formulation utilizes a liquid delivery system. Marketed by P & L Development, Llc, this product is identified by NDC 49580-0385 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
49580-0385-2
Package Description
118 mL in 1 BOTTLE, PLASTIC
Product Code
49580-0385
11-Digit Billing Format
49580038502
RxNorm Crosswalk
  • RxCUI: 1605844 - dextromethorphan HBr 20 MG / guaiFENesin 200 MG in 10 mL Oral Suspension
  • RxCUI: 1605844 - dextromethorphan hydrobromide 2 MG/ML / guaifenesin 20 MG/ML Oral Suspension
  • RxCUI: 1605844 - dextromethorphan HBr 20 MG / guaifenesin 200 MG per 10 ML Oral Suspension

Clinical Specifications

Proprietary Name
Tussin Dm Cough And Chest Congestion Adult
Non-Proprietary Name
Dextromethorphan Hbr, Guaifenesin
Substance Name
Dextromethorphan Hydrobromide; Guaifenesin
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
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Do not take more than 6 doses in any 24-hour periodmeasure only with the dosing cup provided. do not use any other dosing devicekeep dosing cup with productmL= milliliterthis adult product is not intended for use in children under 12 years of ageadults and children 12 years and over: 10 mL every 4 hourschildren under 12 years: do not use

Regulatory & Marketing

Labeler Name
P & L Development, Llc
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
03-31-2015
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (49580-0385). Click a package code to view its specific billing and regulatory data.

49580-0385-4
1 BOTTLE, PLASTIC in 1 BOX / 118 mL in 1 BOTTLE, PLASTIC
49580-0385-8
1 BOTTLE, PLASTIC in 1 BOX / 237 mL in 1 BOTTLE, PLASTIC

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 49580-0385-2 identifies a specific commercial package of 118 ml in 1 bottle, plastic of Tussin Dm Cough And Chest Congestion Adult, a human over the counter drug labeled by P & L Development, Llc. This liquid is formulated for oral use and contains dextromethorphan hydrobromide; guaifenesin as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by P & L Development, Llc on March 31, 2015. The current certification is valid through December 31, 2026.

How is this P & L Development, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 49580038502. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
49580-0385-2
11-Digit CMS (5-4-2)
49580-0385-02

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.