Diflorasone Diacetate
NDC Package 72919-549-60

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.

Diflorasone Diacetate is diflorasone is used to treat a variety of skin conditions (e.g., eczema, dermatitis, allergies, rash). Marketed by Emerald Therapeutics, Llc, this product is identified by NDC 72919-549 and is authorized under FDA application ANDA075508.

Identification & Billing

NDC Package Code
72919-549-60
Package Description
1 TUBE in 1 CARTON / 60 g in 1 TUBE
Product Code
72919-549
11-Digit Billing Format
72919054960
Billing Unit
GM - Billing unit of "gram" is used when a product is measured by its weight.
Units Per Package
60 GM

Clinical Specifications

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

Regulatory & Marketing

Labeler Name
Emerald Therapeutics, Llc
FDA Application #
ANDA075508
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
04-24-2000
End Marketing Date
08-31-2025
Listing Expiration
08-31-2025
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 72919-549-60 identifies a specific commercial package of 1 tube in 1 carton / 60 g in 1 tube of Diflorasone Diacetate, labeled by Emerald Therapeutics, Llc. This product is billed per "GM" gram and contains an estimated amount of 60 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 Emerald Therapeutics, Llc on April 24, 2000. The current certification is valid through August 31, 2025.

What are the primary indications for this medication?

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

How is this Emerald Therapeutics, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72919054960. Quantities are measured in per "gm or gram", products billed per gram are products measured by weight.. There are 60 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)
72919-549-60
11-Digit CMS (5-4-2)
72919-0549-60

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