Roxybond Patent Expiration

Roxybond is a drug owned by Protega Pharmaceuticals Inc. It is protected by 2 US drug patents filed from 2017 to 2019 out of which none have expired yet. Based on its patents and exclusivities, its generic launch date is estimated to be Aug 12, 2028. Details of Roxybond'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).
US7955619 Abuse resistant drugs, method of use and method of making
Aug, 2028

(3 years from now)

Active
US10314788 Pharmaceutical compositions configured to deter dosage form splitting
Aug, 2028

(3 years from now)

Active


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

Exclusivity Information

Roxybond holds 1 exclusivities. All of its exclusivities have expired in 2020. Details of Roxybond's exclusivity codes and their expiration dates are given below.


Drug Exclusivity Drug Exclusivity Expiration
New Product(NP) Apr 20, 2020

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

Roxybond's Family Patents

Roxybond has patent protection in a total of 10 countries. It has a significant patent presence in the US with 60.9% of its patents being US patents. 1 country has all of their patents expired or invalidated which has opened up potential generic launch opportunities in this particular country. Click below to unlock the full patent family tree for Roxybond.

Family Patents

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Generic Launch

Generic Release Date:

Roxybond's generic launch date based on the last expiry date of its patents and exclusivities combined is estimated to be Aug 12, 2028 (This date is subject to change depending upon the patent filing activities by the drug owner or exclusivity additions to its drug application)

Roxybond Generic API suppliers:

Oxycodone Hydrochloride is the generic name for the brand Roxybond. 26 different companies have already filed for the generic of Roxybond, with Epic Pharma Llc having the maximum number of approved applications. Check out the entire list of companies who have already received approval for Roxybond's generic

Alternative Brands for Roxybond

There are several other brand drugs using the same active ingredient (Oxycodone Hydrochloride) as Roxybond. 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
Mallinckrodt Inc
Xartemis Xr
Pfizer
Troxyca Er
Purdue Pharma Lp
Oxycontin
Targiniq
Zyla
Oxaydo


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





About Roxybond

Roxybond is a drug owned by Protega Pharmaceuticals Inc. Roxybond uses Oxycodone Hydrochloride as an active ingredient. Roxybond was launched by Protega Pharms in 2017.

Approval Date:

Roxybond was approved by FDA for market use on 20 April, 2017.

Active Ingredient:

Roxybond uses Oxycodone Hydrochloride as the active ingredient. Check out other Drugs and Companies using Oxycodone Hydrochloride ingredient

Dosage:

Roxybond is available in tablet form for oral use. Given below is detailed information on Dosage -

Strength Dosage Form Availability Application Pathway
15MG TABLET Prescription ORAL
30MG TABLET Prescription ORAL
5MG TABLET Prescription ORAL
10MG TABLET Prescription ORAL