| 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
|
||
|
More 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 |
|---|---|---|---|---|---|
| ******* | *** \ ** | *** *, **** | ******* ***** ****** ** ** | ********* ******** | ** ***** **, **** |
| *** ****** | ** \ ** | **** **, **** | ******* ***** ****** ** ** | ********* ******** | ** ***** **, **** |
| ****** | ** \ ** | *** **, **** | ******* | ******** | ******** ** *** **, **** |
Download ParaIV Report
| Drug Name | Generic Name | Dosage | Route of Administration | Probable FTF | Known Para IV Filers | Other ANDA Developers |
|---|