NDC Package 72835-501-02 Lmr Plus

Lidocaine Kit - View Billable Units, 11-Digit Format, RxNorm

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:
72835-501-02
Package Description:
1 KIT in 1 CARTON * 30 POUCH in 1 CARTON (0591-3525-30) / 1 g in 1 POUCH * 85 g in 1 BOTTLE, PLASTIC (61577-3235-5)
Product Code:
Proprietary Name:
Lmr Plus
Non-Proprietary Name:
Lidocaine
Usage Information:
This product is used to help reduce itching and pain from certain skin conditions (such as scrapes, minor skin irritations, insect bites). It may also be used to help relieve nerve pain after shingles (infection with herpes zoster virus). Lidocaine belongs to a class of drugs known as local anesthetics. It works by causing a temporary loss of feeling in the area where you apply the patch.
11-Digit NDC Billing Format:
72835050102
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
  • RxCUI: 1745091 - lidocaine 5 % Medicated Patch
  • RxCUI: 1745091 - lidocaine 0.05 MG/MG Medicated Patch
  • RxCUI: 415976 - menthol 6 % Topical Gel
  • RxCUI: 415976 - menthol 0.06 MG/MG Topical Gel
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    V2 Pharma, Llc
    Dosage Form:
    Kit - A packaged collection of related material.
    Sample Package:
    No
    FDA Application Number:
    ANDA200675
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    06-03-2019
    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 72835-501-02?

    The NDC Packaged Code 72835-501-02 is assigned to a package of 1 kit in 1 carton * 30 pouch in 1 carton (0591-3525-30) / 1 g in 1 pouch * 85 g in 1 bottle, plastic (61577-3235-5) of Lmr Plus, a human prescription drug labeled by V2 Pharma, Llc. The product's dosage form is kit and is administered via form.

    Is NDC 72835-501 included in the NDC Directory?

    Yes, Lmr Plus with product code 72835-501 is active and included in the NDC Directory. The product was first marketed by V2 Pharma, Llc on June 03, 2019 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 72835-501-02?

    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 72835-501-02?

    The 11-digit format is 72835050102. 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
    5-3-272835-501-025-4-272835-0501-02