Eloxatin Patent Expiration

Eloxatin is a drug owned by Sanofi Aventis Us Llc. It is protected by 8 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 Feb 09, 2017. Details of Eloxatin'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).
US5420319

(Pediatric)

Cis-oxalato(trans-1-1,2-cyclohexanediamine) Pt(II) complex having high optical purity and process of preparing same
Feb, 2017

(7 years ago)

Expired
US5420319 Cis-oxalato(trans-1-1,2-cyclohexanediamine) Pt(II) complex having high optical purity and process of preparing same
Aug, 2016

(8 years ago)

Expired
US5716988

(Pediatric)

Pharmaceutically stable preparation of oxaliplatinum
Feb, 2016

(8 years ago)

Expired
US5716988 Pharmaceutically stable preparation of oxaliplatinum
Aug, 2015

(9 years ago)

Expired
US5338874

(Pediatric)

Cis oxalato (trans 1-1,2-cyclohexanediamine) PT(II) having optically high purity
Oct, 2013

(11 years ago)

Expired
US5290961

(Pediatric)

Platinum compound and process of preparing same
Jul, 2013

(11 years ago)

Expired
US5338874 Cis oxalato (trans 1-1,2-cyclohexanediamine) PT(II) having optically high purity
Apr, 2013

(11 years ago)

Expired
US5290961 Platinum compound and process of preparing same
Jan, 2013

(11 years ago)

Expired

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

Eloxatin's Family Patents


Family Patents

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Generic Launch

Generic Release Date:

Eloxatin's generic launch date based on the expiry of its last outstanding patent is estimated to be Feb 09, 2017 (This date is subject to change depending upon the patent filing activities by the drug owner or exclusivity additions to its drug application)

Eloxatin Generic API suppliers:

Oxaliplatin is the generic name for the brand Eloxatin. 20 different companies have already filed for the generic of Eloxatin, with Fresenius Kabi Usa having the maximum number of approved applications. Check out the entire list of companies who have already received approval for Eloxatin's generic

How can I launch a generic of Eloxatin before its drug patent expiration? :

You can seek FDA approval to launch a generic drug before the expiration of Eloxatin's patents related by providing a 'paragraph IV certification' in your application, which states that the patent submitted by the Eloxatin's sponsor is invalid, unenforceable, or will not be infringed by your generic product.

Given below are the details of the already filed Para IV certificates on Eloxatin -

Strength Submission Date ANDA(s) Filed First applicant approval Last patent expiry 180 day status
5 mg/mL, 10 mL and 20 mL vials 09 Feb, 2007 11 07 Aug, 2009 09 Feb, 2017 Eligible
5 mg/mL, 40 mL vials 16 Jul, 2007 1 07 Aug, 2015 Extinguished





About Eloxatin

Eloxatin is a drug owned by Sanofi Aventis Us Llc. It is used for treating symptoms of depression, anxiety disorders, panic disorders, and certain types of pain. Eloxatin uses Oxaliplatin as an active ingredient. Eloxatin was launched by Sanofi Aventis Us in 2005.

Approval Date:

Eloxatin was approved by FDA for market use on 31 January, 2005.

Active Ingredient:

Eloxatin uses Oxaliplatin as the active ingredient. Check out other Drugs and Companies using Oxaliplatin ingredient

Treatment:

Eloxatin is used for treating symptoms of depression, anxiety disorders, panic disorders, and certain types of pain.

Dosage:

Eloxatin is available in injectable form for intravenous use. Given below is detailed information on Dosage -

Strength Dosage Form Availability Application Pathway
100MG/20ML (5MG/ML) INJECTABLE Discontinued INTRAVENOUS
100MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** INJECTABLE Discontinued INTRAVENOUS
50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** INJECTABLE Discontinued INTRAVENOUS
50MG/10ML (5MG/ML) INJECTABLE Discontinued INTRAVENOUS
200MG/40ML (5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** INJECTABLE Discontinued INTRAVENOUS