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  5. NDC Package Code: 72483-100-04 Resfridol Antitussive

NDC Package 72483-100-04 Resfridol Antitussive

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:
72483-100-04
Package Description:
1 BOTTLE in 1 BOX / 120 mL in 1 BOTTLE
Product Code:
72483-100
Proprietary Name:
Resfridol Antitussive
Usage Information:
Do not exceed recommended dosagedo not exceed 4 doses in a 24-hour periodadults & children 12 year of age & over: 1 teaspoonful (10 mL), every 6 hourschildren 6 to under 12 years of age: 1/2 teaspoonful (5 mL), every 6 hourschildren under 6 years of age: do not use
11-Digit NDC Billing Format:
72483010004
NDC to RxNorm Crosswalk:
  • RxCUI: 2280291 - dextromethorphan HBr 30 MG / guaiFENesin 200 MG in 10 mL Oral Suspension
  • RxCUI: 2280291 - dextromethorphan hydrobromide 3 MG/ML / guaifenesin 20 MG/ML Oral Suspension
  • RxCUI: 2280291 - dextromethorphan HBr 3 MG/ML / guaifenesin 20 MG/ML Oral Suspension
  • RxCUI: 2280291 - dextromethorphan HBr 30 MG / guaifenesin 200 MG per 10 ML Oral Suspension
    • Labeler Name:
    Laboratorios Alfa
    Sample Package:
    No
    Start Marketing Date:
    08-01-2019
    Listing Expiration Date:
    12-31-2023
    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 72483-100-04?

    The NDC Packaged Code 72483-100-04 is assigned to a package of 1 bottle in 1 box / 120 ml in 1 bottle of Resfridol Antitussive, labeled by Laboratorios Alfa. The product's dosage form is and is administered via form.

    Is NDC 72483-100 included in the NDC Directory?

    No, Resfridol Antitussive with product code 72483-100 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Laboratorios Alfa on August 01, 2019 and its listing in the NDC Directory is set to expire on December 31, 2023 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 72483-100-04?

    The 11-digit format is 72483010004. 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
    5-3-272483-100-045-4-272483-0100-04