Fluticasone Propionate Powder, Metered
NDC Package 50090-7962-0

11-digit billing NDC: 50090796200 · Billing unit: EA · 1 EA per package
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Fluticasone Propionate powders is fluticasone Propionate DISKUS is indicated for the maintenance treatment of asthma as prophylactic therapy in patients aged 4 years and older.Important Limitation of UseFluticasone Propionate DISKUS is NOT indicated for the relief of acute bronchospasm. This formulation utilizes a powder, metered delivery system. Marketed by A-s Medication Solutions, this product is identified by NDC 50090-7962 and is authorized under FDA application NDA020833.

Identification & Billing

NDC Package Code
50090-7962-0
Package Description
1 INHALER in 1 CARTON / 60 POWDER, METERED in 1 INHALER
Product Code
50090-7962
11-Digit Billing Format
50090796200
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
1 EA
RxNorm Crosswalk
  • RxCUI: 896021 - fluticasone propionate 100 MCG/INHAL Dry Powder Inhaler, 60 Blisters
  • RxCUI: 896021 - 60 ACTUAT fluticasone propionate 0.1 MG/ACTUAT Dry Powder Inhaler
  • RxCUI: 896021 - fluticasone propionate 0.1 MG/ACTUAT Dry Powder Inhaler, 60 ACTUAT

Clinical Specifications

Proprietary Name
Fluticasone Propionate Diskus
Non-Proprietary Name
Fluticasone Propionate
Substance Name
Fluticasone Propionate
Dosage Form
Powder, Metered - An powder dosage form that is situated inside a container that has a mechanism to deliver a specified quantity.
Administration Route
Respiratory (inhalation) - Administration within the respiratory tract by inhaling orally or nasally for local or systemic effect.
Active Ingredient(s)
FLUTICASONE PROPIONATE 100 ug/1
Pharmacologic Class
Usage Information
Fluticasone Propionate DISKUS is indicated for the maintenance treatment of asthma as prophylactic therapy in patients aged 4 years and older.Important Limitation of UseFluticasone Propionate DISKUS is NOT indicated for the relief of acute bronchospasm.

Regulatory & Marketing

Labeler Name
A-s Medication Solutions
Product Type
Human Prescription Drug
FDA Application #
NDA020833
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
10-30-2023
Listing Expiration
12-31-2027
Exclude Flag
N
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 50090-7962-0 identifies a specific commercial package of 1 inhaler in 1 carton / 60 powder, metered in 1 inhaler of Fluticasone Propionate Diskus, a human prescription drug labeled by A-s Medication Solutions. This product is billed for "EA" each discreet unit and contains an estimated amount of 1 billable units per package. This powder, metered is formulated for respiratory (inhalation) use and contains fluticasone propionate as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by A-s Medication Solutions on October 30, 2023. The current certification is valid through December 31, 2027.

How is this A-s Medication Solutions product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 50090796200. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 1 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)
50090-7962-0
11-Digit CMS (5-4-2)
50090-7962-00

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