Betamethasone Dipropionate
NDC Package 63187-433-15

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

Package Information

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

Betamethasone Dipropionate is a medication used to treat a variety of skin conditions (e.g., eczema, dermatitis, allergies, rash). Marketed by Proficient Rx Lp, this product is identified by NDC 63187-433 and is authorized under FDA application ANDA078930.

Identification & Billing

NDC Package Code
63187-433-15
Package Description
15 g in 1 TUBE
Product Code
63187-433
11-Digit Billing Format
63187043315
RxNorm Crosswalk
  • RxCUI: 848176 - betamethasone 0.05 % (betamethasone dipropionate 0.064 % ) Augmented Topical Cream
  • RxCUI: 848176 - Augmented betamethasone 0.5 MG/ML Topical Cream
  • RxCUI: 848176 - augmented betamethasone 0.05 % Topical Cream

Clinical Specifications

Proprietary Name
Betamethasone Dipropionate
Dosage Form
-
Usage Information
This medication is used to treat a variety of skin conditions (e.g., eczema, dermatitis, allergies, rash). Betamethasone reduces the swelling, itching, and redness that can occur in these types of conditions. This medication is a strong corticosteroid.

Regulatory & Marketing

Labeler Name
Proficient Rx Lp
FDA Application #
ANDA078930
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
09-23-2008
Listing Expiration
12-31-2018
Exclude Flag
I
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 63187-433-15 identifies a specific commercial package of 15 g in 1 tube of Betamethasone Dipropionate, labeled by Proficient Rx Lp. 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 Proficient Rx Lp on September 23, 2008. The current certification is valid through December 31, 2018.

What are the primary indications for this medication?

This medication is used to treat a variety of skin conditions (e.g., eczema, dermatitis, allergies, rash). Betamethasone reduces the swelling, itching, and redness that can occur in these types of conditions. This medication is a strong corticosteroid.

How is this Proficient Rx Lp product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 63187043315. 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)
63187-433-15
11-Digit CMS (5-4-2)
63187-0433-15

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