Olux-e
NDC Package 40076-101-50

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Olux-e is a medication used to treat a variety of skin conditions (e.g., psoriasis, eczema, dermatitis, allergies, rash). Marketed by Prestium Pharma, Inc., this product is identified by NDC 40076-101 and is authorized under FDA application NDA022013.

Identification & Billing

NDC Package Code
40076-101-50
Package Description
50 g in 1 CAN
Product Code
40076-101
11-Digit Billing Format
40076010150
Billing Unit
GM - Billing unit of "gram" is used when a product is measured by its weight.
Units Per Package
50 GM

Clinical Specifications

Proprietary Name
Olux-e
Dosage Form
-
Usage Information
This medication is used to treat a variety of skin conditions (e.g., psoriasis, eczema, dermatitis, allergies, rash). Clobetasol reduces the swelling, itching, and redness that can occur in these types of conditions. It also can heal the rough, scaly patches on the skin seen with psoriasis. Clobetasol is a very strong (super-high-potency) corticosteroid. This medication also contains emollients. Emollients soften and moisturize the skin, leading to decreased itching and flaking. Emollients also help to protect the skin against irritation. This medication is not recommended for use in children younger than 12 years.

Regulatory & Marketing

Labeler Name
Prestium Pharma, Inc.
FDA Application #
NDA022013
Marketing Category
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date
02-12-2007
End Marketing Date
07-31-2020
Listing Expiration
07-31-2020
Exclude Flag
D
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (40076-101). Click a package code to view its specific billing and regulatory data.

40076-101-00
100 g in 1 CAN

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 40076-101-50 identifies a specific commercial package of 50 g in 1 can of Olux-e, labeled by Prestium Pharma, Inc.. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Prestium Pharma, Inc. on February 12, 2007. The current certification is valid through July 31, 2020.

What are the primary indications for this medication?

This medication is used to treat a variety of skin conditions (e.g., psoriasis, eczema, dermatitis, allergies, rash). Clobetasol reduces the swelling, itching, and redness that can occur in these types of conditions. It also can heal the rough, scaly patches on the skin seen with psoriasis. Clobetasol is a very strong (super-high-potency) corticosteroid. This medication also contains emollients. Emollients soften and moisturize the skin, leading to decreased itching and flaking. Emollients also help to protect the skin against irritation. This medication is not recommended for use in children younger than 12 years.

How is this Prestium Pharma, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 40076010150. Quantities are measured in per "gm or gram", products billed per gram are products measured by weight.. There are 50 total billable units per package. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
40076-101-50
11-Digit CMS (5-4-2)
40076-0101-50

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.