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  5. NDC Package Code: 75940-121-30 Conazol

NDC Package 75940-121-30 Conazol

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
75940-121-30
Package Description:
30 g in 1 TUBE
Product Code:
75940-121
Proprietary Name:
Conazol
Usage Information:
Wash the affected area and dry thoroughlyapply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctorsupervise children in the use of this productfor athlete's foot, pay special attention to the spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once dailyfor the athlete's foot and ringworm, use daily for 4 weeksfor jock itch, use daily for 2 weeksnot effective on the scalp or nails
11-Digit NDC Billing Format:
75940012130
NDC to RxNorm Crosswalk:
  • RxCUI: 2121948 - Conazol Antifungal 2 % Topical Cream
  • RxCUI: 2121948 - miconazole nitrate 20 MG/ML Topical Cream [Conazol Miconazole]
  • RxCUI: 2121948 - Conazol Miconazole 20 MG/ML Topical Cream
  • RxCUI: 998483 - miconazole nitrate 2 % Topical Cream
  • RxCUI: 998483 - miconazole nitrate 20 MG/ML Topical Cream
    • Labeler Name:
    Marcasusa Llc
    Sample Package:
    No
    Start Marketing Date:
    08-01-2014
    Listing Expiration Date:
    12-31-2020
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    75940-121-022 g in 1 PACKET
    75940-121-46130 g in 1 CAN

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 75940-121-30?

    The NDC Packaged Code 75940-121-30 is assigned to a package of 30 g in 1 tube of Conazol, labeled by Marcasusa Llc. The product's dosage form is and is administered via form.

    Is NDC 75940-121 included in the NDC Directory?

    No, Conazol with product code 75940-121 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Marcasusa Llc on August 01, 2014 and its listing in the NDC Directory is set to expire on December 31, 2020 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 75940-121-30?

    The 11-digit format is 75940012130. 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
    5-3-275940-121-305-4-275940-0121-30