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  5. NDC Package Code: 0023-6118-03 Condylox

NDC Package 0023-6118-03 Condylox

Podofilox Gel Topical - 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:
0023-6118-03
Package Description:
3.5 g in 1 TUBE, WITH APPLICATOR
Product Code:
0023-6118
Proprietary Name:
Condylox
Non-Proprietary Name:
Podofilox
Substance Name:
Podofilox
Usage Information:
This medication is used on the skin to treat external genital warts.
11-Digit NDC Billing Format:
00023611803
Billing Unit:
GM - Billing unit of "gram" is used when a product is measured by its weight.
NDC to RxNorm Crosswalk:
3.5 GM
NDC to RxNorm Crosswalk:
  • RxCUI: 312466 - podofilox 0.5 % Topical Gel
  • RxCUI: 312466 - podofilox 0.005 MG/MG Topical Gel
  • RxCUI: 312466 - podophyllotoxin 0.5 % Topical Gel
  • RxCUI: 351750 - Condylox 0.5 % Topical Gel
  • RxCUI: 351750 - podofilox 0.005 MG/MG Topical Gel [Condylox]
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Allergan, Inc.
    Dosage Form:
    Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
    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):
  • PODOFILOX 5 mg/g
    • Pharmacologic Class(es):
  • Decreased Mitosis - [PE] (Physiologic Effect)
    • Sample Package:
    No
    FDA Application Number:
    NDA020529
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    03-13-1997
    Listing Expiration Date:
    12-31-2025
    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 0023-6118-03?

    The NDC Packaged Code 0023-6118-03 is assigned to a package of 3.5 g in 1 tube, with applicator of Condylox, a human prescription drug labeled by Allergan, Inc.. The product's dosage form is gel and is administered via topical form.

    Is NDC 0023-6118 included in the NDC Directory?

    Yes, Condylox with product code 0023-6118 is active and included in the NDC Directory. The product was first marketed by Allergan, Inc. on March 13, 1997 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 0023-6118-03?

    The contents of this package are billed per "gm or gram", products billed per gram are products measured by weight. The calculated billable units for this package is 3.5.

    What is the 11-digit format for NDC 0023-6118-03?

    The 11-digit format is 00023611803. 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 4-4-2 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
    4-4-20023-6118-035-4-200023-6118-03