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  5. NDC Package Code: 71598-200-15 Bupropidex

NDC Package 71598-200-15 Bupropidex

Dextromethorphan Hydrobromide Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
71598-200-15
Package Description:
200 TABLET in 1 BOTTLE
Product Code:
71598-200
Proprietary Name:
Bupropidex
Non-Proprietary Name:
Dextromethorphan Hydrobromide
Substance Name:
Dextromethorphan Hydrobromide
Usage Information:
This product is used as Cough suppressant. Temporarily relieves cough due to minor throat and bronchial irritation as may occur with the common cold.
11-Digit NDC Billing Format:
71598020015
NDC to RxNorm Crosswalk:
  • RxCUI: 2173733 - dextromethorphan HBr 15 MG Oral Tablet
  • RxCUI: 2173733 - dextromethorphan hydrobromide 15 MG Oral Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Dxm Pharmacuetical, Inc.
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • DEXTROMETHORPHAN HYDROBROMIDE 15 mg/1
    • Pharmacologic Class(es):
  • Sigma-1 Agonist - [EPC] (Established Pharmacologic Class)
  • Sigma-1 Receptor Agonists - [MoA] (Mechanism of Action)
  • Uncompetitive N-methyl-D-aspartate Receptor Antagonist - [EPC] (Established Pharmacologic Class)
  • Uncompetitive NMDA Receptor Antagonists - [MoA] (Mechanism of Action)
    • Sample Package:
    No
    FDA Application Number:
    M013
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    12-01-2023
    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 71598-200-15?

    The NDC Packaged Code 71598-200-15 is assigned to a package of 200 tablet in 1 bottle of Bupropidex, a human over the counter drug labeled by Dxm Pharmacuetical, Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 71598-200 included in the NDC Directory?

    Yes, Bupropidex with product code 71598-200 is active and included in the NDC Directory. The product was first marketed by Dxm Pharmacuetical, Inc. on December 01, 2023 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 71598-200-15?

    The 11-digit format is 71598020015. 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
    5-3-271598-200-155-4-271598-0200-15