NDC Package 37808-518-25 Maximum Strength Dm Max

Dextromethorphan Hydrobromide,Guaifenesin Liquid 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:
37808-518-25
Package Description:
177 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Maximum Strength Dm Max
Non-Proprietary Name:
Dextromethorphan Hydrobromide, Guaifenesin
Substance Name:
Dextromethorphan Hydrobromide; Guaifenesin
Usage Information:
Uses• helps loosen phlegm (mucus)and thin bronchial secretions todrain bronchial tubes• temporarily relieves thesesymploms occurring with a cold:    • cough due to minor throat and      bronchial irritation
11-Digit NDC Billing Format:
37808051825
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
  • Product Type:
    Human Otc Drug
    Labeler Name:
    H E B
    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.
  • Sample Package:
    No
    FDA Application Number:
    M012
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    09-14-2012
    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 37808-518-25?

    The NDC Packaged Code 37808-518-25 is assigned to a package of 177 ml in 1 bottle of Maximum Strength Dm Max, a human over the counter drug labeled by H E B. The product's dosage form is liquid and is administered via oral form.

    Is NDC 37808-518 included in the NDC Directory?

    Yes, Maximum Strength Dm Max with product code 37808-518 is active and included in the NDC Directory. The product was first marketed by H E B on September 14, 2012 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 37808-518-25?

    The 11-digit format is 37808051825. 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
    5-3-237808-518-255-4-237808-0518-25