Flurandrenolide
NDC Package 51672-5301-4

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 discontinued by the firm.

Flurandrenolide is a medication used to treat a variety of skin conditions (e.g., eczema, dermatitis, allergies, rash). Marketed by Sun Pharmaceutical Industries, Inc., this product is identified by NDC 51672-5301 and is authorized under FDA application NDA012806.

Identification & Billing

NDC Package Code
51672-5301-4
Package Description
1 TUBE in 1 CARTON / 120 g in 1 TUBE
Product Code
51672-5301
11-Digit Billing Format
51672530104
Billing Unit
GM - Billing unit of "gram" is used when a product is measured by its weight.
Units Per Package
120 GM

Clinical Specifications

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

Regulatory & Marketing

Labeler Name
Sun Pharmaceutical Industries, Inc.
FDA Application #
NDA012806
Marketing Category
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date
04-25-2016
End Marketing Date
01-31-2023
Listing Expiration
01-31-2023
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 51672-5301-4 identifies a specific commercial package of 1 tube in 1 carton / 120 g in 1 tube of Flurandrenolide, labeled by Sun Pharmaceutical Industries, Inc.. This product is billed per "GM" gram and contains an estimated amount of 120 billable units per package. 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 Sun Pharmaceutical Industries, Inc. on April 25, 2016. The current certification is valid through January 31, 2023.

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). Flurandrenolide reduces the swelling, itching and redness that can occur in these types of conditions. This medication is a medium-strength corticosteroid.

How is this Sun Pharmaceutical Industries, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 51672530104. Quantities are measured in per "gm or gram", products billed per gram are products measured by weight.. There are 120 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 (5-4-1)
51672-5301-4
11-Digit CMS (5-4-2)
51672-5301-04

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