NDC Package 99207-850-02 Luzu

Luliconazole Cream Topical - 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:
99207-850-02
Package Description:
12 TUBE in 1 CARTON / 2 g in 1 TUBE
Product Code:
Proprietary Name:
Luzu
Non-Proprietary Name:
Luliconazole
Substance Name:
Luliconazole
Usage Information:
Luliconazole is used to treat skin infections such as athlete's foot, jock itch, and ringworm. Luliconazole is an azole antifungal that works by preventing the growth of the fungus.
11-Digit NDC Billing Format:
99207085002
NDC to RxNorm Crosswalk:
  • RxCUI: 1482684 - luliconazole 1 % Topical Cream
  • RxCUI: 1482684 - luliconazole 10 MG/ML Topical Cream
  • RxCUI: 1482689 - Luzu 1 % Topical Cream
  • RxCUI: 1482689 - luliconazole 10 MG/ML Topical Cream [Luzu]
  • RxCUI: 1482689 - Luzu 10 MG/ML Topical Cream
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Bausch Health Us, Llc
    Dosage Form:
    Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
    Administration Route(s):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Active Ingredient(s):
    Sample Package:
    Yes
    FDA Application Number:
    NDA204153
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    11-14-2013
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    99207-850-601 TUBE in 1 CARTON / 60 g in 1 TUBE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 99207-850-02?

    The NDC Packaged Code 99207-850-02 is assigned to a package of 12 tube in 1 carton / 2 g in 1 tube of Luzu, a human prescription drug labeled by Bausch Health Us, Llc. The product's dosage form is cream and is administered via topical form.

    Is NDC 99207-850 included in the NDC Directory?

    Yes, Luzu with product code 99207-850 is active and included in the NDC Directory. The product was first marketed by Bausch Health Us, Llc on November 14, 2013 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 11-digit format for NDC 99207-850-02?

    The 11-digit format is 99207085002. 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
    5-3-299207-850-025-4-299207-0850-02