Quzyttir Patent Expiration

Quzyttir is a drug owned by Jdp Therapeutics Llc. It is protected by 5 US drug patents filed in 2019 out of which none have expired yet. Based on its patents and exclusivities, its generic launch date is estimated to be Feb 28, 2030. Details of Quzyttir'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).
US8314083 Non-sedating antihistamine injection formulations and methods of use thereof
Feb, 2030

(5 years from now)

Active
US8263581 Non-sedating antihistamine injection formulations and methods of use thereof
Feb, 2030

(5 years from now)

Active
US9180090 Non-sedating antihistamine injection formulations and methods of use thereof
Feb, 2030

(5 years from now)

Active
US8513259 Non-sedating antihistamine injection formulations and methods of use thereof
Feb, 2030

(5 years from now)

Active
US9119771 Non-sedating antihistamine injection formulations and methods of use thereof
Feb, 2030

(5 years from now)

Active


A patent's expiry date may change depending upon legal activities going on that patent. Critical activities like abandoning of a patent, term extension of a patent or amendment of its claims can increase or decrease the life of a patent hence affecting its expiry date and in turn affecting the generic launch date of that drug. Tracking these ongoing activities on a patent application helps to keep an eye on the latest developments in the patent process of the drug which can give an idea of how early a drug's generic could be available. The next section provides a list of recent legal activities on Quzyttir's patents.

Given below is the list of recent legal activities going on the following patents of Quzyttir.

Activity Date Patent Number
Patent litigations
Payment of Maintenance Fee, 12th Year, Large Entity 08 May, 2024 US8314083
Payment of Maintenance Fee, 12th Year, Large Entity 28 Feb, 2024 US8263581
Payment of Maintenance Fee, 8th Year, Large Entity 15 Feb, 2023 US9119771
Entity Status Set To Undiscounted (Initial Default Setting or Status Change) 23 Apr, 2021 US9119771
Entity Status Set To Undiscounted (Initial Default Setting or Status Change) 23 Apr, 2021 US8314083
Entity Status Set To Undiscounted (Initial Default Setting or Status Change) 23 Apr, 2021 US8513259
Payment of Maintenance Fee, 8th Yr, Small Entity 15 Jan, 2021 US8513259
Payment of Maintenance Fee, 8th Yr, Small Entity 15 Apr, 2020 US8314083
Payment of Maintenance Fee, 8th Year, Large Entity 15 Apr, 2020 US8263581
7.5 yr surcharge - late pmt w/in 6 mo, Large Entity 15 Apr, 2020 US8263581


FDA has granted several exclusivities to Quzyttir. Till the time these exclusivities are active, no other company can market a generic or bioequivalent version of Quzyttir, 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 Quzyttir.

Exclusivity Information

Quzyttir holds 1 exclusivities. All of its exclusivities have expired in 2022. Details of Quzyttir's exclusivity codes and their expiration dates are given below.


Drug Exclusivity Drug Exclusivity Expiration
New Product(NP) Oct 04, 2022

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US patents provide insights into the exclusivity only within the United States, but Quzyttir 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 Quzyttir's family patents as well as insights into ongoing legal events on those patents.

Quzyttir's Family Patents

Quzyttir has patent protection in a total of 5 countries. It has a significant patent presence in the US with 73.3% of its patents being US patents. Click below to unlock the full patent family tree for Quzyttir.

Family Patents

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Generic Launch

Generic Release Date:

Quzyttir's generic launch date based on the last expiry date of its patents and exclusivities combined is estimated to be Feb 28, 2030 (This date is subject to change depending upon the patent filing activities by the drug owner or exclusivity additions to its drug application)

Quzyttir Generic API suppliers:

Cetirizine Hydrochloride is the generic name for the brand Quzyttir. 47 different companies have already filed for the generic of Quzyttir, with Taro having the maximum number of approved applications. Check out the entire list of companies who have already received approval for Quzyttir's generic

Alternative Brands for Quzyttir

Quzyttir which is used for the treatment of acute urticaria and angioedema by increasing peak plasma concentration through intravenous injection., has several other brand drugs using the same active ingredient (Cetirizine Hydrochloride). 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 Cetirizine Hydrochloride, Quzyttir's active ingredient. Check the complete list of approved generic manufacturers for Quzyttir





About Quzyttir

Quzyttir is a drug owned by Jdp Therapeutics Llc. It is used for the treatment of acute urticaria and angioedema by increasing peak plasma concentration through intravenous injection. Quzyttir uses Cetirizine Hydrochloride as an active ingredient. Quzyttir was launched by Jdp in 2019.

Approval Date:

Quzyttir was approved by FDA for market use on 04 October, 2019.

Active Ingredient:

Quzyttir uses Cetirizine Hydrochloride as the active ingredient. Check out other Drugs and Companies using Cetirizine Hydrochloride ingredient

Treatment:

Quzyttir is used for the treatment of acute urticaria and angioedema by increasing peak plasma concentration through intravenous injection.

Dosage:

Quzyttir is available in solution form for intravenous use. Given below is detailed information on Dosage -

Strength Dosage Form Availability Application Pathway
10MG/ML (10MG/ML) SOLUTION Prescription INTRAVENOUS