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  5. NDC Package Code: 72835-802-02 Duloxicaine

NDC Package 72835-802-02 Duloxicaine

Duloxetine And Lidocaine 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:
72835-802-02
Package Description:
1 KIT in 1 CARTON * 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-295-06) * 96.4 g in 1 TUBE (86089-200-01)
Product Code:
72835-802
Proprietary Name:
Duloxicaine
Non-Proprietary Name:
Duloxetine And Lidocaine
Usage Information:
• Adults and children over 12 years: Apply as needed to affected areas 3-4 times a day. Consult a physician if pain persists.  • Children 12 years of younger: consult a doctor
11-Digit NDC Billing Format:
72835080202
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
  • RxCUI: 1010895 - lidocaine HCl 4 % Topical Cream
  • RxCUI: 1010895 - lidocaine hydrochloride 40 MG/ML Topical Cream
  • RxCUI: 1010895 - lidocaine hydrochloride 4 % Topical Cream
  • RxCUI: 2597529 - Lidocream Plus 4 % Topical Cream
  • RxCUI: 2597529 - lidocaine hydrochloride 40 MG/ML Topical Cream [Lidocream]
    • 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:
    01-23-2023
    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 72835-802-02?

    The NDC Packaged Code 72835-802-02 is assigned to a package of 1 kit in 1 carton * 30 capsule, delayed release in 1 bottle (68180-295-06) * 96.4 g in 1 tube (86089-200-01) of Duloxicaine, a human prescription drug labeled by V2 Pharma, Llc. The product's dosage form is kit and is administered via form.

    Is NDC 72835-802 included in the NDC Directory?

    Yes, Duloxicaine with product code 72835-802 is active and included in the NDC Directory. The product was first marketed by V2 Pharma, Llc on January 23, 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 NDC billing unit for package 72835-802-02?

    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 72835-802-02?

    The 11-digit format is 72835080202. 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
    5-3-272835-802-025-4-272835-0802-02