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  5. NDC Package Code: 72835-601-02 Quinixil

NDC Package 72835-601-02 Quinixil

Mometasone Furoate And Dimethicone 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:
72835-601-02
Package Description:
1 KIT in 1 CARTON * 1 TUBE in 1 CARTON (0713-0634-37) / 45 g in 1 TUBE * 114 g in 1 TUBE (69740-322-00)
Product Code:
72835-601
Proprietary Name:
Quinixil
Non-Proprietary Name:
Mometasone Furoate And Dimethicone
Usage Information:
Mometasone furoate cream 0.1% is a corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses in patients ≥ 2 years of age. (1)
11-Digit NDC Billing Format:
72835060102
Billing Unit:
GM - Billing unit of "gram" is used when a product is measured by its weight.
NDC to RxNorm Crosswalk:
  • RxCUI: 259090 - dimethicone 5 % Topical Cream
  • RxCUI: 259090 - dimethicone 50 MG/ML Topical Cream
  • RxCUI: 311753 - mometasone furoate 0.1 % Topical Cream
  • RxCUI: 311753 - mometasone furoate 1 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
    FDA Application Number:
    ANDA076216
    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 72835-601-02?

    The NDC Packaged Code 72835-601-02 is assigned to a package of 1 kit in 1 carton * 1 tube in 1 carton (0713-0634-37) / 45 g in 1 tube * 114 g in 1 tube (69740-322-00) of Quinixil, a human prescription drug labeled by V2 Pharma, Llc. The product's dosage form is kit and is administered via form.

    Is NDC 72835-601 included in the NDC Directory?

    Yes, Quinixil with product code 72835-601 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 72835-601-02?

    The contents of this package are billed per "gm or gram", products billed per gram are products measured by weight.

    What is the 11-digit format for NDC 72835-601-02?

    The 11-digit format is 72835060102. 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
    5-3-272835-601-025-4-272835-0601-02