NDC Package 10631-119-01 Ultravate X

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
10631-119-01
Package Description:
1 KIT in 1 KIT * 50 g in 1 TUBE (10631-102-50) * 225 g in 1 TUBE (10631-114-05)
Product Code:
Proprietary Name:
Ultravate X
Usage Information:
Ultravate Ointment 0.05% is a super-high potency corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses. Treatment beyond two consecutive weeks is not recommended, and the total dosage should not exceed 50 g/week because of the potential for the drug to suppress the hypothalamic-pituitary-adrenal (HPA) axis. Use in children under 12 years of age is not recommended.As with other highly active corticosteroids, therapy should be discontinued when control has been achieved. If no improvement is seen within 2 weeks, reassessment of the diagnosis may be necessary.
11-Digit NDC Billing Format:
10631011901
Billing Unit:
GM - Billing unit of "gram" is used when a product is measured by its weight.
NDC to RxNorm Crosswalk:
  • RxCUI: 1041718 - ammonium lactate 10 % Topical Cream
  • RxCUI: 1041718 - ammonium lactate 100 MG/ML Topical Cream
  • RxCUI: 1041718 - ammonium lactate (as neutralized lactic acid) 10 % Topical Cream
  • RxCUI: 1301695 - {1 (50000 MG) (halobetasol propionate 0.0005 MG/MG Topical Ointment) / 1 (225000 MG) (lactic acid 100 MG/ML Topical Cream) } Pack
  • RxCUI: 1301695 - halobetasol propionate 0.05 % Topical Ointment (50 GM) / lactid acid 10 % Topical Cream (225 GM Pack)
  • Labeler Name:
    Ranbaxy Laboratories Inc.
    Sample Package:
    No
    Start Marketing Date:
    07-01-2012
    Listing Expiration Date:
    12-31-2017
    Exclude Flag:
    I
    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 10631-119-01?

    The NDC Packaged Code 10631-119-01 is assigned to a package of 1 kit in 1 kit * 50 g in 1 tube (10631-102-50) * 225 g in 1 tube (10631-114-05) of Ultravate X, labeled by Ranbaxy Laboratories Inc.. The product's dosage form is and is administered via form.

    Is NDC 10631-119 included in the NDC Directory?

    No, Ultravate X with product code 10631-119 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Ranbaxy Laboratories Inc. on July 01, 2012 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 10631-119-01?

    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 10631-119-01?

    The 11-digit format is 10631011901. 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
    5-3-210631-119-015-4-210631-0119-01