Lopinavir and Ritonavir | Abbvie | ||
200mg; 50mg,100mg; 25mg ,Tablet, Oral |
Less Than $1000 mn
|
||
Less Than 5
|
Less Than 5
|
||
More Than 5
|
Less Than 5
|
||
Less Than 5
|
Less Than 5
|
||
Indicated in combination with other antiretroviral agents for the treatment of HIV1 infection in adults and pediatric patients | |||
Yes
|
Kaletra | Patent 1 | Patent 2 | Patent 3 | Patent 4 | Patent 5 | Patent 6 | Patent 7 | Patent 8 | Patent 9 |
---|---|---|---|---|---|---|---|---|---|
***** (******) | ******* | **** *** | ******* | ******* | ******* | ******* | ******* | ******* | ******* |
****** | ******* | ******* | **** *** | ******* | ******* | ******* | ******* | ******* | ******* |
********* | ******* | **** *** | ******* | ******* | ******* | ******* | ******* | ******* | ******* |
Company | FTF Status / 180 days exclusivity | 30-Months stay | Current Litigation Status | Current Approval Status | Likelihood of launch |
---|---|---|---|---|---|
***** (******) | *** \ ** | ****, **** | ******* | ******** | *** ****** ******* |
****** | ** \ ** | ***** *, **** | ******* | ******** | ******** ** *** *, **** |
********* | ** \ ** | **** **, **** | ******* | ********* ******** | ****** **** ******** |
Lopinavir and Ritonavir | Abbott | ||
80mg/20mg per ml; oral solution |
Less Than $1000 mn
|
||
Less Than 5
|
Less Than 5
|
||
More Than 5
|
Less Than 5
|
||
Less Than 5
|
Less Than 5
|
||
Indicated in combination with other antiretroviral agents for the treatment of HIV-1 infection in adults and pediatric patients 14 days and older. | |||
Yes
|
Kaletra | 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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