NDC Package 0591-4039-74 Clobetasol Propionate

Spray Topical - View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is approaching its end of marketing date. An upcoming end of marketing date means the product has been delisted but will remain in the NDC database until the end of marketing date is reached. In most cases, the FDA advises firms to use the expiration date of the last lot produced as the end marketing date, reflecting the possibility that the product may still be available even after manufacturing has stopped.

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:
0591-4039-74
Package Description:
1 BOTTLE in 1 CARTON / 125 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Clobetasol Propionate
Non-Proprietary Name:
Clobetasol Propionate
Substance Name:
Clobetasol Propionate
Usage Information:
This medication is used to treat a variety of skin conditions (e.g., eczema, psoriasis, dermatitis, allergies, rash). Clobetasol 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:
00591403974
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:
Actavis Pharma, Inc.
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 AUTHORIZED GENERIC - A product marketed as a "generic" drug under an approved New Drug Application (NDA), rather than an Abbreviated New Drug Application (ANDA),.
Start Marketing Date:
08-28-2015
End Marketing Date:
09-30-2025
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.

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Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
0591-4039-461 BOTTLE in 1 CARTON / 59 mL in 1 BOTTLE

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Frequently Asked Questions

What is NDC 0591-4039-74?

The NDC Packaged Code 0591-4039-74 is assigned to a package of 1 bottle in 1 carton / 125 ml in 1 bottle of Clobetasol Propionate, a human prescription drug labeled by Actavis Pharma, Inc.. The product's dosage form is spray and is administered via topical form.

Is NDC 0591-4039 included in the NDC Directory?

Yes, Clobetasol Propionate with product code 0591-4039 is active and included in the NDC Directory. The product was first marketed by Actavis Pharma, Inc. on August 28, 2015.

What is the NDC billing unit for package 0591-4039-74?

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 0591-4039-74?

The 11-digit format is 00591403974. 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
4-4-20591-4039-745-4-200591-4039-74