Advair Diskus 250/50 Patent Expiration

Advair Diskus 250/50 is a drug owned by Glaxo Group Ltd England Dba Glaxosmithkline. It is protected by 2 US drug patents filed in 2013 out of which all have expired. Based on its patents and exclusivities, its generic launch date is estimated to be Dec 20, 2020. Details of Advair Diskus 250/50's patents and their expiration are given in the table below.

Drug Patent Number Drug Patent Title Drug Patent Expiry Status
These drug patents focus on the other aspects of the drug like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US5873360

(Pediatric)

Inhalation device
Aug, 2016

(8 years ago)

Expired
US5873360 Inhalation device
Feb, 2016

(8 years ago)

Expired


FDA has granted several exclusivities to Advair Diskus 250/50. Till the time these exclusivities are active, no other company can market a generic or bioequivalent version of Advair Diskus 250/50, regardless of the status of it's patents. These exclusivities hence play a crucial role in delaying the generic launch. Given below are details of the exclusivities granted to Advair Diskus 250/50.

Exclusivity Information

Advair Diskus 250/50 holds 2 exclusivities. All of its exclusivities have expired in 2020. Details of Advair Diskus 250/50's exclusivity codes and their expiration dates are given below.


Drug Exclusivity Drug Exclusivity Expiration
M(M-84) Mar 31, 2012
M(M-214) Dec 20, 2020

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US patents provide insights into the exclusivity only within the United States, but Advair Diskus 250/50 is protected by patents in multiple countries. Understanding the full scope of patent protection is crucial in strategizing market entry. By looking at the broader patent landscape, you can identify markets with weaker patent protection which could be ideal generic entry points. The following section offers details on Advair Diskus 250/50's family patents as well as insights into ongoing legal events on those patents.

Advair Diskus 250/50's Family Patents


Family Patents

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Generic Launch

Generic Release Date:

Advair Diskus 250/50's generic launch date based on the last expiry date of its patents and exclusivities combined is estimated to be Dec 20, 2020 (This date is subject to change depending upon the patent filing activities by the drug owner or exclusivity additions to its drug application)

Advair Diskus 250/50 Generic API suppliers:

Fluticasone Propionate; Salmeterol Xinafoate is the generic name for the brand Advair Diskus 250/50. 3 different companies have already filed for the generic of Advair Diskus 250/50, with Hikma having the maximum number of approved applications. Check out the entire list of companies who have already received approval for Advair Diskus 250/50's generic

Alternative Brands for Advair Diskus 250/50

There are several other brand drugs using the same active ingredient (Fluticasone Propionate; Salmeterol Xinafoate) as Advair Diskus 250/50. Given below is the list of those companies and their brand drugs, to help you identify new opportunities, assess competitors, and plan your market strategies more effectively.


Apart from brand drugs containing the same ingredient, some generics have also been filed for Fluticasone Propionate; Salmeterol Xinafoate, Advair Diskus 250/50's active ingredient. Check the complete list of approved generic manufacturers for Advair Diskus 250/50





About Advair Diskus 250/50

Advair Diskus 250/50 is a drug owned by Glaxo Group Ltd England Dba Glaxosmithkline. Advair Diskus 250/50 uses Fluticasone Propionate; Salmeterol Xinafoate as an active ingredient. Advair Diskus 250/50 was launched by Glaxo Grp Ltd in 2000.

Approval Date:

Advair Diskus 250/50 was approved by FDA for market use on 24 August, 2000.

Active Ingredient:

Advair Diskus 250/50 uses Fluticasone Propionate; Salmeterol Xinafoate as the active ingredient. Check out other Drugs and Companies using Fluticasone Propionate; Salmeterol Xinafoate ingredient

Dosage:

Advair Diskus 250/50 is available in powder form for inhalation use. Given below is detailed information on Dosage -

Strength Dosage Form Availability Application Pathway
0.25MG/INH;EQ 0.05MG BASE/INH POWDER Prescription INHALATION