NDC Package 53943-504-26 Tussin Cf

Dextromethorphan Hydrobromide,Guaifenesin,Phenylephrine Hydrochloride 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:
53943-504-26
Package Description:
237 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Tussin Cf
Non-Proprietary Name:
Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
Substance Name:
Dextromethorphan Hydrobromide; Guaifenesin; Phenylephrine Hydrochloride
Usage Information:
Do not take more than 6 doses in any 24 hour periodThis adult strength product is not intended for use in children under 12 years of age Age Dose adults and children 12 years and over 2 teaspoons every 4 hours children under 12 do not use
11-Digit NDC Billing Format:
53943050426
NDC to RxNorm Crosswalk:
  • RxCUI: 1044949 - dextromethorphan HBr 20 MG / guaiFENesin 200 MG / phenylephrine HCl 10 MG in 10 mL Oral Solution
  • RxCUI: 1044949 - dextromethorphan hydrobromide 2 MG/ML / guaifenesin 20 MG/ML / phenylephrine hydrochloride 1 MG/ML Oral Solution
  • RxCUI: 1044949 - dextromethorphan HBr 10 MG / guaifenesin 100 MG / phenylephrine HCl 5 MG per 5 ML Oral Solution
  • RxCUI: 1044949 - dextromethorphan HBr 20 MG / guaifenesin 200 MG / phenylephrine HCl 10 MG per 10 ML Oral Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Discount Drug Mart
    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:
    11-19-2014
    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 53943-504-26?

    The NDC Packaged Code 53943-504-26 is assigned to a package of 237 ml in 1 bottle of Tussin Cf, a human over the counter drug labeled by Discount Drug Mart. The product's dosage form is liquid and is administered via oral form.

    Is NDC 53943-504 included in the NDC Directory?

    Yes, Tussin Cf with product code 53943-504 is active and included in the NDC Directory. The product was first marketed by Discount Drug Mart on November 19, 2014 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 53943-504-26?

    The 11-digit format is 53943050426. 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
    5-3-253943-504-265-4-253943-0504-26