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  5. NDC Package Code: 72835-302-02 Podiatrole

NDC Package 72835-302-02 Podiatrole

Ketoconazole 2% And Urea 20% Kit - 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:
72835-302-02
Package Description:
1 KIT in 1 CARTON * 1 TUBE in 1 BOX (GS1:3005361109455) / 85 g in 1 TUBE * 1 TUBE in 1 CARTON (51672-1298-2) / 30 g in 1 TUBE
Product Code:
72835-302
Proprietary Name:
Podiatrole
Non-Proprietary Name:
Ketoconazole 2% And Urea 20%
Usage Information:
Do not use if known hypersensitivity to any of the listed ingredients of any of the components included on the kit. Ketoconazole cream, 2% is contraindicated in persons who have shown hypersensitivity to the active or excipient ingredients of this formulation.
11-Digit NDC Billing Format:
72835030202
NDC to RxNorm Crosswalk:
  • RxCUI: 198886 - urea 20 % Topical Cream
  • RxCUI: 198886 - urea 200 MG/ML Topical Cream
  • RxCUI: 198886 - urea 17 GM in 85 GM Topical Cream
  • RxCUI: 203088 - ketoconazole 2 % Topical Cream
  • RxCUI: 203088 - ketoconazole 20 MG/ML Topical Cream
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    V2 Pharma, Llc
    Dosage Form:
    Kit - A packaged collection of related material.
    Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    01-06-2023
    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 72835-302-02?

    The NDC Packaged Code 72835-302-02 is assigned to a package of 1 kit in 1 carton * 1 tube in 1 box (gs1:3005361109455) / 85 g in 1 tube * 1 tube in 1 carton (51672-1298-2) / 30 g in 1 tube of Podiatrole, a human prescription drug labeled by V2 Pharma, Llc. The product's dosage form is kit and is administered via form.

    Is NDC 72835-302 included in the NDC Directory?

    Yes, Podiatrole with product code 72835-302 is active and included in the NDC Directory. The product was first marketed by V2 Pharma, Llc on January 06, 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 72835-302-02?

    The 11-digit format is 72835030202. 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
    5-3-272835-302-025-4-272835-0302-02