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

Here are the details of the already filed Para IV certificates on ABILIFY:-

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

Here are the details of the already filed Para IV certificates on ABRAXANE:-

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

Here are the details of the already filed Para IV certificates on ACETADOTE:-

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

Here are the details of the already filed Para IV certificates on ACTOPLUS MET XR:-

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

Here are the details of the already filed Para IV certificates on ADEMPAS:-

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

Here are the details of the already filed Para IV certificates on ADZENYS XR-ODT:-

A supplementary protection certificate (SPC) is a type of intellectual property right granted in the European Union. It provides an extension of the term of protection for a medicinal product that has been authorized for sale in the EU, beyond the 20-year term provided by the basic patent.

The aim of SPCs is to compensate for the time taken to get regulatory approval for a new drug, and to provide an incentive for companies to invest in research and development in the field of medicinal products.

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

Here are the details of the already filed Para IV certificates on AFINITOR:-

A supplementary protection certificate (SPC) is a type of intellectual property right granted in the European Union. It provides an extension of the term of protection for a medicinal product that has been authorized for sale in the EU, beyond the 20-year term provided by the basic patent.

The aim of SPCs is to compensate for the time taken to get regulatory approval for a new drug, and to provide an incentive for companies to invest in research and development in the field of medicinal products.

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

Here are the details of the already filed Para IV certificates on APLENZIN:-

A supplementary protection certificate (SPC) is a type of intellectual property right granted in the European Union. It provides an extension of the term of protection for a medicinal product that has been authorized for sale in the EU, beyond the 20-year term provided by the basic patent.

The aim of SPCs is to compensate for the time taken to get regulatory approval for a new drug, and to provide an incentive for companies to invest in research and development in the field of medicinal products.

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

Here are the details of the already filed Para IV certificates on APTIOM:-

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

Here are the details of the already filed Para IV certificates on ARICEPT:-

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

Here are the details of the already filed Para IV certificates on ATELVIA:-

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

Here are the details of the already filed Para IV certificates on ATRIPLA:-

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

Here are the details of the already filed Para IV certificates on AUBAGIO:-

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

Here are the details of the already filed Para IV certificates on AXIRON:-

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

Here are the details of the already filed Para IV certificates on BELEODAQ:-

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

Here are the details of the already filed Para IV certificates on BELRAPZO:-

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

Here are the details of the already filed Para IV certificates on BENDEKA:-

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

Here are the details of the already filed Para IV certificates on BOSULIF:-

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

Here are the details of the already filed Para IV certificates on BRIDION:-