Konvomep Patent Expiration

Konvomep is a drug owned by Azurity Pharmaceuticals Inc. It is protected by 6 US drug patents filed from 2022 to 2024 out of which none have expired yet. Based on its patents and exclusivities, its generic launch date is estimated to be Mar 01, 2040. Details of Konvomep'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).
US11771686 Compositions and kits for omeprazole suspension
Mar, 2040

(15 years from now)

Active
US11911473 Compositions and kits for omeprazole suspension
Jul, 2039

(14 years from now)

Active
US10751333 Compositions and kits for omeprazole suspension
Jul, 2039

(14 years from now)

Active
US11103492 Compositions and kits for omeprazole suspension
Jul, 2039

(14 years from now)

Active
US11633478 Compositions and kits for Omeprazole suspension
Jul, 2039

(14 years from now)

Active
US12042539 Compositions and kits for Omeprazole suspension
Jul, 2039

(14 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 Konvomep's patents.

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

Activity Date Patent Number
Patent litigations
Mail Patent eGrant Notification 27 Feb, 2024 US11911473
Email Notification 27 Feb, 2024 US11911473
Patent Issue Date Used in PTA Calculation 27 Feb, 2024 US11911473
Patent eGrant Notification 27 Feb, 2024 US11911473
Recordation of Patent Grant Mailed 27 Feb, 2024 US11911473
Recordation of Patent eGrant 27 Feb, 2024 US11911473
Payment of Maintenance Fee, 4th Year, Large Entity 26 Feb, 2024 US10751333
Email Notification 08 Feb, 2024 US11911473
Issue Notification Mailed 07 Feb, 2024 US11911473
Application Is Considered Ready for Issue 23 Jan, 2024 US11911473

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

Konvomep's Family Patents

Konvomep has patent protection in a total of 4 countries. It has a significant patent presence in the US with 66.7% of its patents being US patents. Click below to unlock the full patent family tree for Konvomep.

Family Patents

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Generic Launch

Generic Release Date:

Konvomep's generic launch date based on the expiry of its last outstanding patent is estimated to be Mar 01, 2040 (This date is subject to change depending upon the patent filing activities by the drug owner or exclusivity additions to its drug application)

Konvomep Generic API suppliers:

Omeprazole; Sodium Bicarbonate is the generic name for the brand Konvomep. 11 different companies have already filed for the generic of Konvomep, with Strides Pharma having the maximum number of approved applications. Check out the entire list of companies who have already received approval for Konvomep's generic

Alternative Brands for Konvomep

Konvomep which is used for reducing the risk of upper gastrointestinal bleeding and short-term treatment of active benign gastric ulcers in critically ill patients., has several other brand drugs in the same treatment category and using the same active ingredient (Omeprazole; Sodium Bicarbonate). 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.

Drug Owner Drug Name Treatment Area
Salix
Zegerid

(uses Omeprazole; Sodium Bicarbonate)

Used for treatment of upper gastrointestinal issues including ulcers, GERD symptoms, and maintenance of esophagitis healing.
Santarus
Zegerid

(uses Omeprazole; Sodium Bicarbonate)

Used for treatment of upper gastrointestinal issues including ulcers, GERD symptoms, and maintenance of esophagitis healing.

Apart from drugs working in same treatment category, there are also some brand drugs where treatment area is different, but the active ingredient used is same i.e. Omeprazole; Sodium Bicarbonate. Given below is the list of those drugs and companies owning them.



Apart from brand drugs containing the same ingredient, some generics have also been filed for Omeprazole; Sodium Bicarbonate, Konvomep's active ingredient. Check the complete list of approved generic manufacturers for Konvomep





About Konvomep

Konvomep is a drug owned by Azurity Pharmaceuticals Inc. It is used for reducing the risk of upper gastrointestinal bleeding and short-term treatment of active benign gastric ulcers in critically ill patients. Konvomep uses Omeprazole; Sodium Bicarbonate as an active ingredient. Konvomep was launched by Azurity in 2022.

Approval Date:

Konvomep was approved by FDA for market use on 30 August, 2022.

Active Ingredient:

Konvomep uses Omeprazole; Sodium Bicarbonate as the active ingredient. Check out other Drugs and Companies using Omeprazole; Sodium Bicarbonate ingredient

Treatment:

Konvomep is used for reducing the risk of upper gastrointestinal bleeding and short-term treatment of active benign gastric ulcers in critically ill patients.

Dosage:

Konvomep is available in for suspension form for oral use. Given below is detailed information on Dosage -

Strength Dosage Form Availability Application Pathway
2MG/ML;84MG/ML FOR SUSPENSION Prescription ORAL