Oxcarbazepine | SUPERNUS PHARMS | ||
150, 300 mg; Tablet, Extended Release |
Less Than $1000 mn
|
||
Less Than 5
|
More Than 5
|
||
More Than 5
|
Less Than 5
|
||
Less Than 5
|
Less Than 5
|
||
Indicated for the treatment of partial-onset seizures in patients 6 years of age and older. | |||
Yes
|
Oxtellar XR | Patent 1 | Patent 2 | Patent 3 | Patent 4 | Patent 5 | Patent 6 | Patent 7 | Patent 8 | Patent 9 | Patent 10 | Patent 11 |
---|---|---|---|---|---|---|---|---|---|---|---|
******* | ******* ***** **** ** ** | ******* ***** **** ** ** | ******* ***** **** ** ** | ******* | ******* | ******* | ******* | ******* | ******* | *** ********* (***** ******) | *** ********* (***** ******) |
*** ****** | ******* ***** **** ** ** | ******* ***** **** ** ** | ******* | ******* ***** **** ** ** | ******* | ******* | ******* | ******* | ******* | *** ********* (***** ******) | *** ********* (***** ******) |
****** | ******* | ******* | ******* | ******* | ******* | ******* | ******* | ******* | ******* | ******* (***** ******) | *** ********* (***** ******) |
Company | FTF Status / 180 days exclusivity | 30-Months stay | Current Litigation Status | Current Approval Status | Likelihood of launch |
---|---|---|---|---|---|
******* | *** \ ** | *** *, **** | ******* ***** ****** ** ** | ********* ******** | ** ***** **, **** |
*** ****** | ** \ ** | **** **, **** | ******* ***** ****** ** ** | ********* ******** | ** ***** **, **** |
****** | ** \ ** | *** **, **** | ******* | ******** | ******** ** *** **, **** |
Oxcarbazepine | SUPERNUS PHARMS | ||
600 mg; Tablet, Extended Release |
Less Than $1000 mn
|
||
Less Than 5
|
More Than 5
|
||
Less Than 5
|
Less Than 5
|
||
Less Than 5
|
Less Than 5
|
||
Oxtellar XR is indicated for the treatment of partial-onset seizures in patients 6 years of age and older | |||
Yes
|
Oxtellar XR | Patent 1 | Patent 2 | Patent 3 | Patent 4 | Patent 5 | Patent 6 | Patent 7 | Patent 8 | Patent 9 | Patent 10 | Patent 11 |
---|---|---|---|---|---|---|---|---|---|---|---|
******* | ******* ***** **** ** ** | ******* ***** **** ** ** | ******* ***** **** ** ** | ******* | ******* | ******* | ******* | ******* | ******* | *** ********* (***** ******) | *** ********* (***** ******) |
*** ****** | ******* ***** **** ** ** | ******* ***** **** ** ** | ******* | ******* ***** **** ** ** | ******* | ******* | ******* | ******* | ******* | *** ********* (***** ******) | *** ********* (***** ******) |
****** | ******* | ******* | ******* | ******* | ******* | ******* | ******* | ******* | ******* | ******* (***** ******) | *** ********* (***** ******) |
Company | FTF Status / 180 days exclusivity | 30-Months stay | Current Litigation Status | Current Approval Status | Likelihood of launch |
---|---|---|---|---|---|
******* | *** \ ** | *** *, **** | ******* ***** ****** ** ** | ********* ******** | ** ***** **, **** |
*** ****** | ** \ ** | **** **, **** | ******* ***** ****** ** ** | ********* ******** | ** ***** **, **** |
****** | ** \ ** | *** **, **** | ******* | ******** | ******** ** *** **, **** |
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Drug Name | Generic Name | Dosage | Route of Administration | Probable FTF | Known Para IV Filers | Other ANDA Developers |
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