NDC Package 76519-1177-0 Flovent Diskus

View Billable Units, 11-Digit Format, RxNorm

Package Information

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

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:
76519-1177-0
Package Description:
60 POWDER, METERED in 1 INHALER
Product Code:
Proprietary Name:
Flovent Diskus
Usage Information:
Fluticasone is used to control and prevent symptoms (such as wheezing and shortness of breath) caused by asthma. It works by reducing swelling (inflammation) of the airways in the lungs to make breathing easier. Controlling symptoms of asthma helps you maintain your normal activities and decreases time lost from work or school. Fluticasone belongs to a class of drugs known as corticosteroids. This medication must be used regularly to be effective. It does not work right away and should not be used to relieve sudden asthma attacks. If an asthma attack occurs, use your quick-relief inhaler (such as albuterol, also called salbutamol in some countries) as prescribed.
11-Digit NDC Billing Format:
76519117700
NDC to 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
  • RxCUI: 896023 - Flovent Diskus 100 MCG/INHAL Dry Powder Inhaler, 60 Blisters
  • RxCUI: 896023 - 60 ACTUAT fluticasone propionate 0.1 MG/ACTUAT Dry Powder Inhaler [Flovent]
Labeler Name:
H.j. Harkins Company, Inc.
Sample Package:
No
FDA Application Number:
NDA020833
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
04-23-2019
Listing Expiration Date:
12-31-2021
Exclude Flag:
I
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.

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 76519-1177-0?

The NDC Packaged Code 76519-1177-0 is assigned to a package of 60 powder, metered in 1 inhaler of Flovent Diskus, labeled by H.j. Harkins Company, Inc.. The product's dosage form is and is administered via form.

Is NDC 76519-1177 included in the NDC Directory?

No, Flovent Diskus with product code 76519-1177 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by H.j. Harkins Company, Inc. on April 23, 2019 and its listing in the NDC Directory is set to expire on December 31, 2021 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 76519-1177-0?

The 11-digit format is 76519117700. 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 5-4-1 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
5-4-176519-1177-05-4-276519-1177-00