NDC Package 0187-0002-03 Bryhali

Halobetasol Propionate Lotion 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:
0187-0002-03
Package Description:
1 TUBE in 1 CARTON / 3 g in 1 TUBE
Product Code:
Proprietary Name:
Bryhali
Non-Proprietary Name:
Halobetasol Propionate
Substance Name:
Halobetasol Propionate
Usage Information:
This medication is used to treat a variety of skin conditions (such as eczema, dermatitis, psoriasis, rash). Halobetasol reduces the swelling, itching, and redness that can occur in these types of conditions. This medication is a very strong (super-high potency) corticosteroid.
11-Digit NDC Billing Format:
00187000203
NDC to RxNorm Crosswalk:
  • RxCUI: 2101710 - halobetasol propionate 0.01 % Topical Lotion
  • RxCUI: 2101710 - halobetasol propionate 0.1 MG/ML Topical Lotion
  • RxCUI: 2101715 - Bryhali 0.01 % Topical Lotion
  • RxCUI: 2101715 - halobetasol propionate 0.1 MG/ML Topical Lotion [Bryhali]
  • RxCUI: 2101715 - Bryhali 0.1 MG/ML Topical Lotion
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Bausch Health Us, Llc
    Dosage Form:
    Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
    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:
    NDA209355
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    11-06-2018
    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
    0187-0002-011 TUBE in 1 CARTON / 100 g in 1 TUBE
    0187-0002-601 TUBE in 1 CARTON / 60 g in 1 TUBE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0187-0002-03?

    The NDC Packaged Code 0187-0002-03 is assigned to a package of 1 tube in 1 carton / 3 g in 1 tube of Bryhali, a human prescription drug labeled by Bausch Health Us, Llc. The product's dosage form is lotion and is administered via topical form.

    Is NDC 0187-0002 included in the NDC Directory?

    Yes, Bryhali with product code 0187-0002 is active and included in the NDC Directory. The product was first marketed by Bausch Health Us, Llc on November 06, 2018 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 0187-0002-03?

    The 11-digit format is 00187000203. 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
    4-4-20187-0002-035-4-200187-0002-03