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  5. NDC Package Code: 49580-0505-6 Mucus Relief Dm Maximum Strength

NDC Package 49580-0505-6 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:
49580-0505-6
Package Description:
177 mL in 1 BOTTLE, PLASTIC
Product Code:
49580-0505
Proprietary Name:
Mucus Relief Dm Maximum Strength
Usage Information:
Do not take more than 6 doses in any 24-hour period measure only with dosing cup provided. Do not use any other dosing device keep dosing cup with product mL = milliliter dose as follows or as directed by a doctor adults and children 12 years of age and older: 20 mL every 4 hours children under 12 years of age: do not use
11-Digit NDC Billing Format:
49580050506
NDC to RxNorm Crosswalk:
  • RxCUI: 1020138 - dextromethorphan HBr 20 MG / guaiFENesin 400 MG in 20 mL Oral Solution
  • RxCUI: 1020138 - dextromethorphan hydrobromide 1 MG/ML / guaifenesin 20 MG/ML Oral Solution
  • RxCUI: 1020138 - dextromethorphan HBr 20 MG / guaifenesin 400 MG per 20 ML Oral Solution
  • RxCUI: 1020138 - dextromethorphan HBr 5 MG / guaifenesin 100 MG per 5 ML Oral Solution
    • Labeler Name:
    P & L Development, Llc
    Sample Package:
    No
    Start Marketing Date:
    04-30-2016
    Listing Expiration Date:
    12-31-2022
    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 49580-0505-6?

    The NDC Packaged Code 49580-0505-6 is assigned to a package of 177 ml in 1 bottle, plastic of Mucus Relief Dm Maximum Strength, labeled by P & L Development, Llc. The product's dosage form is and is administered via form.

    Is NDC 49580-0505 included in the NDC Directory?

    No, Mucus Relief Dm Maximum Strength with product code 49580-0505 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by P & L Development, Llc on April 30, 2016 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 49580-0505-6?

    The 11-digit format is 49580050506. 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
    5-4-149580-0505-65-4-249580-0505-06