Oraverse Patent Expiration

Oraverse is a drug owned by Septodont Holding Sas. It is protected by 5 US drug patents filed in 2013. Out of these, 1 drug patents are active and 4 have expired. Based on its patents and exclusivities, its generic launch date is estimated to be Apr 21, 2025. Details of Oraverse'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).
US7575757 Stabilized formulations of alpha adrenergic receptor antagonists and the uses thereof
Apr, 2025

(4 months from now)

Active
US7569230 Stabilized formulations of alpha adrenergic receptor antagonists and the uses thereof
Oct, 2023

(1 year, 2 months ago)

Expired
US7229630 Stabilized formulations of alpha adrenergic receptor antagonists and the uses thereof
Jun, 2023

(1 year, 5 months ago)

Expired
US6872390 Local anesthetic methods and kits
May, 2021

(3 years ago)

Expired
US6764678 Local anesthetic methods and kits
May, 2021

(3 years ago)

Expired


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 Oraverse's patents.

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

Activity Date Patent Number
Patent litigations
Payment of Maintenance Fee, 12th Year, Large Entity 08 Feb, 2021 US7575757
Payment of Maintenance Fee, 12th Year, Large Entity 25 Jan, 2021 US7569230
Payment of Maintenance Fee, 12th Year, Large Entity 03 Dec, 2018 US7229630
Termination or Final Written Decision 06 Nov, 2016 US7575757
Petition Requesting Trial 06 Nov, 2016 US7575757
Request for Trial Granted in Part 06 Nov, 2016 US7575757
Request for Trial Granted 08 Jul, 2016 US7575757
Petition Requesting Trial 08 Jul, 2016 US7575757
Entity Status Set To Undiscounted (Initial Default Setting or Status Change) 30 Dec, 2010 US7229630
Recordation of Patent Grant Mailed 18 Aug, 2009 US7575757


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

Exclusivity Information

Oraverse holds 1 exclusivities. All of its exclusivities have expired in 2019. Details of Oraverse's exclusivity codes and their expiration dates are given below.


Drug Exclusivity Drug Exclusivity Expiration
New Patient Population(NPP) Mar 18, 2019

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

Oraverse's Family Patents

Oraverse has patent protection in a total of 12 countries. It's US patent count contributes only to 43.5% of its total global patent coverage. 5 countries have all of their patents expired or invalidated which has opened up potential generic launch opportunities in these countries. Click below to unlock the full patent family tree for Oraverse.

Family Patents

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Generic Launch

Generic Release Date:

Oraverse's generic launch date based on the last expiry date of its patents and exclusivities combined is estimated to be Apr 21, 2025 (This date is subject to change depending upon the patent filing activities by the drug owner or exclusivity additions to its drug application)

Oraverse Generic API suppliers:

Phentolamine Mesylate is the generic name for the brand Oraverse. 2 different companies have already filed for the generic of Oraverse, with Hikma having the maximum number of approved applications. Check out the entire list of companies who have already received approval for Oraverse's generic

Alternative Brands for Oraverse

Oraverse which is used for reversal of soft-tissue anesthesia following intraoral local anesthetic injection., has several other brand drugs using the same active ingredient (Phentolamine Mesylate). 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
Famygen Life Sci
Ryzumvi


Apart from brand drugs containing the same ingredient, some generics have also been filed for Phentolamine Mesylate, Oraverse's active ingredient. Check the complete list of approved generic manufacturers for Oraverse





About Oraverse

Oraverse is a drug owned by Septodont Holding Sas. It is used for reversal of soft-tissue anesthesia following intraoral local anesthetic injection. Oraverse uses Phentolamine Mesylate as an active ingredient. Oraverse was launched by Septodont Holding in 2008.

Approval Date:

Oraverse was approved by FDA for market use on 09 May, 2008.

Active Ingredient:

Oraverse uses Phentolamine Mesylate as the active ingredient. Check out other Drugs and Companies using Phentolamine Mesylate ingredient

Treatment:

Oraverse is used for reversal of soft-tissue anesthesia following intraoral local anesthetic injection.

Dosage:

Oraverse is available in injectable form for injection use. Given below is detailed information on Dosage -

Strength Dosage Form Availability Application Pathway
0.4MG/1.7ML INJECTABLE Prescription INJECTION