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  5. NDC Package Code: 73159-008-60 Ultravate

NDC Package 73159-008-60 Ultravate

Halobetasol Propionate Lotion 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:
73159-008-60
Package Description:
1 BOTTLE in 1 CARTON / 59 g in 1 BOTTLE
Product Code:
73159-008
Proprietary Name:
Ultravate
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:
73159000860
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Lacer Pharma, 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):
HALOBETASOL PROPIONATE .5 mg/g
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
NDA208183
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
04-06-2025
Listing Expiration Date:
12-31-2026
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 73159-008-60?

The NDC Packaged Code 73159-008-60 is assigned to a package of 1 bottle in 1 carton / 59 g in 1 bottle of Ultravate, a human prescription drug labeled by Lacer Pharma, Llc. The product's dosage form is lotion and is administered via topical form.

Is NDC 73159-008 included in the NDC Directory?

Yes, Ultravate with product code 73159-008 is active and included in the NDC Directory. The product was first marketed by Lacer Pharma, Llc on April 06, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 73159-008-60?

The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

What is the 11-digit format for NDC 73159-008-60?

The 11-digit format is 73159000860. 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
5-3-273159-008-605-4-273159-0008-60