Podiatrole
NDC Package 72835-302-02

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Podiatrole is do not use if known hypersensitivity to any of the listed ingredients of any of the components included on the kit. Marketed by V2 Pharma, Llc, this product is identified by NDC 72835-302.

Identification & Billing

NDC Package Code
72835-302-02
Package Description
1 KIT in 1 CARTON * 1 TUBE in 1 CARTON (51672-1298-2) / 30 g in 1 TUBE * 1 TUBE in 1 BOX (GS1:3005361109455) / 85 g in 1 TUBE
Product Code
72835-302
11-Digit Billing Format
72835030202
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Podiatrole
Dosage Form
-
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.

Regulatory & Marketing

Labeler Name
V2 Pharma, Llc
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
End Marketing Date
02-08-2023
Listing Expiration
02-08-2023
Exclude Flag
D
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 72835-302-02 identifies a specific commercial package of 1 kit in 1 carton * 1 tube in 1 carton (51672-1298-2) / 30 g in 1 tube * 1 tube in 1 box (gs1:3005361109455) / 85 g in 1 tube of Podiatrole, labeled by V2 Pharma, Llc. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by V2 Pharma, Llc on January 06, 2023. The current certification is valid through February 08, 2023.

How is this V2 Pharma, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72835030202. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
72835-302-02
11-Digit CMS (5-4-2)
72835-0302-02

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.