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  5. NDC Package Code: 75940-122-05 Cicloferon

NDC Package 75940-122-05 Cicloferon

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:
75940-122-05
Package Description:
1 TUBE in 1 CONTAINER / 4 g in 1 TUBE
Product Code:
75940-122
Proprietary Name:
Cicloferon
Usage Information:
Clean the affected areaapply a small amount of this product to the affected area 1 to 3 times dailymay be covered with a sterile bandagechildren under 12 years of age, consult a doctor
11-Digit NDC Billing Format:
75940012205
NDC to RxNorm Crosswalk:
  • RxCUI: 1431682 - benzalkonium chloride 0.13 % / lidocaine HCl 2 % Topical Gel
  • RxCUI: 1431682 - benzalkonium chloride 0.0013 MG/MG / lidocaine hydrochloride 0.02 MG/MG Topical Gel
  • RxCUI: 1431682 - benzalkonium chloride 0.13 % / lidocaine hydrochloride 2 % Topical Gel
  • RxCUI: 1431687 - CICLOFERON 0.13 % / 2 % Topical Gel
  • RxCUI: 1431687 - benzalkonium chloride 0.0013 MG/MG / lidocaine hydrochloride 0.02 MG/MG Topical Gel [Cicloferon]
    • Labeler Name:
    Marcasusa Llc
    Sample Package:
    No
    Start Marketing Date:
    08-01-2011
    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
    75940-122-021 TUBE in 1 CARTON / 2 g in 1 TUBE
    75940-122-041 TUBE in 1 CARTON / 4 g in 1 TUBE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 75940-122-05?

    The NDC Packaged Code 75940-122-05 is assigned to a package of 1 tube in 1 container / 4 g in 1 tube of Cicloferon, labeled by Marcasusa Llc. The product's dosage form is and is administered via form.

    Is NDC 75940-122 included in the NDC Directory?

    No, Cicloferon with product code 75940-122 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, 2011 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 75940-122-05?

    The 11-digit format is 75940012205. 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
    5-3-275940-122-055-4-275940-0122-05