NDC Package 0299-3849-01 Clobex

Clobetasol Propionate Spray 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:
0299-3849-01
Package Description:
1 BOTTLE in 1 CARTON / 10 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Clobex
Non-Proprietary Name:
Clobetasol Propionate
Substance Name:
Clobetasol Propionate
Usage Information:
Clobetasol is used in adults to treat moderate to severe scalp psoriasis. Clobetasol reduces the swelling, itching and redness that can occur with this condition. This medication is a very strong (super-high-potency) corticosteroid. This medication is not recommended for use in children or those less than 18 years of age due to an increased risk of side effects. Consult your doctor or pharmacist for details.
11-Digit NDC Billing Format:
00299384901
NDC to RxNorm Crosswalk:
  • RxCUI: 861512 - clobetasol propionate 0.05 % Topical Spray
  • RxCUI: 861512 - clobetasol propionate 0.5 MG/ML Topical Spray
  • RxCUI: 861513 - Clobex 0.05 % Topical Spray
  • RxCUI: 861513 - clobetasol propionate 0.5 MG/ML Topical Spray [Clobex]
  • RxCUI: 861513 - Clobex 0.5 MG/ML Topical Spray
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Galderma Laboratories, L.p.
    Dosage Form:
    Spray - A liquid minutely divided as by a jet of air or steam.
    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:
    No
    FDA Application Number:
    NDA021835
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    10-27-2005
    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
    0299-3849-021 BOTTLE in 1 CARTON / 59 mL in 1 BOTTLE
    0299-3849-041 BOTTLE in 1 CARTON / 125 mL in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0299-3849-01?

    The NDC Packaged Code 0299-3849-01 is assigned to a package of 1 bottle in 1 carton / 10 ml in 1 bottle of Clobex, a human prescription drug labeled by Galderma Laboratories, L.p.. The product's dosage form is spray and is administered via topical form.

    Is NDC 0299-3849 included in the NDC Directory?

    Yes, Clobex with product code 0299-3849 is active and included in the NDC Directory. The product was first marketed by Galderma Laboratories, L.p. on October 27, 2005 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 0299-3849-01?

    The 11-digit format is 00299384901. 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
    4-4-20299-3849-015-4-200299-3849-01