NDC Package 72835-202-02 Fenovar

Diclofenac Sodium And Menthol,Methyl Salicylate Kit - View Billable Units, 11-Digit Format, RxNorm

Package Information
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:

72835-202-02

Package Description:

1 KIT in 1 CARTON * 1 BOTTLE in 1 CARTON (65162-911-74) / 150 mL in 1 BOTTLE * 85 g in 1 TUBE (51824-105-03)

Product Code:

72835-202

Proprietary Name:

Fenovar

Non-Proprietary Name:

Diclofenac Sodium And Menthol, Methyl Salicylate

Usage Information:

Diclofenac sodium topical solution is indicated for the treatment of signs and symptoms of osteoarthritis of the knee(s).

11-Digit NDC Billing Format:

72835020202

Billing Unit:

EA - Billing unit of "each" is used when the product is dispensed in discreet units.

NDC to RxNorm Crosswalk:

RxCUI: 311498 - menthol 10 % / methyl salicylate 15 % Topical Cream
RxCUI: 311498 - menthol 100 MG/ML / methyl salicylate 150 MG/ML Topical Cream
RxCUI: 311498 - menthol 10 GM / methyl salicylate 15 GM per 100 GM Topical Cream
RxCUI: 857700 - diclofenac sodium 1.5 % Topical Solution
RxCUI: 857700 - diclofenac sodium 15 MG/ML Topical Solution

Product Type:

Human Prescription Drug

Labeler Name:

V2 Pharma, Llc

Dosage Form:

Kit - A packaged collection of related material.

Sample Package:

Marketing Category:

UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.

Start Marketing Date:

01-21-2022

Listing Expiration Date:

12-31-2025

Exclude Flag:

Code Structure:

72835 - V2 Pharma, Llc
- 72835-202 - Fenovar
  - 72835-202-02 - 1 KIT in 1 CARTON * 1 BOTTLE in 1 CARTON (65162-911-74) / 150 mL in 1 BOTTLE * 85 g in 1 TUBE (51824-105-03)

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 72835-202-02?

The NDC Packaged Code 72835-202-02 is assigned to a package of 1 kit in 1 carton * 1 bottle in 1 carton (65162-911-74) / 150 ml in 1 bottle * 85 g in 1 tube (51824-105-03) of Fenovar, a human prescription drug labeled by V2 Pharma, Llc. The product's dosage form is kit and is administered via form.

Is NDC 72835-202 included in the NDC Directory?

Yes, Fenovar with product code 72835-202 is active and included in the NDC Directory. The product was first marketed by V2 Pharma, Llc on January 21, 2022 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 72835-202-02?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units.

What is the 11-digit format for NDC 72835-202-02?

The 11-digit format is 72835020202. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	72835-202-02	5-4-2	72835-0202-02

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