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  5. NDC Package Code: 50458-675-20 Vermox

NDC Package 50458-675-20 Vermox

Mebendazole Tablet, Chewable 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:
50458-675-20
Package Description:
200 TABLET, CHEWABLE in 1 BOTTLE
Product Code:
50458-675
Proprietary Name:
Vermox
Non-Proprietary Name:
Mebendazole
Substance Name:
Mebendazole
Usage Information:
Mebendazole is used to treat intestinal worm infections such as pinworm, roundworm, and hookworm.
11-Digit NDC Billing Format:
50458067520
NDC to RxNorm Crosswalk:
  • RxCUI: 1855385 - mebendazole 500 MG Chewable Tablet
  • RxCUI: 1855387 - Vermox 500 MG Chewable Tablet
  • RxCUI: 1855387 - mebendazole 500 MG Chewable Tablet [Vermox]
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Janssen Pharmaceuticals, Inc.
    Dosage Form:
    Tablet, Chewable - A solid dosage form containing medicinal substances with or without suitable diluents that is intended to be chewed, producing a pleasant tasting residue in the oral cavity that is easily swallowed and does not leave a bitter or unpleasant after-taste.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • MEBENDAZOLE 500 mg/1
    • Pharmacologic Class(es):
  • Anthelmintic - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    NDA208398
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    10-20-2016
    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 50458-675-20?

    The NDC Packaged Code 50458-675-20 is assigned to a package of 200 tablet, chewable in 1 bottle of Vermox, a human prescription drug labeled by Janssen Pharmaceuticals, Inc.. The product's dosage form is tablet, chewable and is administered via oral form.

    Is NDC 50458-675 included in the NDC Directory?

    Yes, Vermox with product code 50458-675 is active and included in the NDC Directory. The product was first marketed by Janssen Pharmaceuticals, Inc. on October 20, 2016 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 50458-675-20?

    The 11-digit format is 50458067520. 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
    5-3-250458-675-205-4-250458-0675-20