NEVIRAPINE |
077429 |
001 |
ANDA |
NEVIRAPINE |
TABLET; ORAL |
200MG |
No
|
No
|
2005/06/20
(TA)
|
--
|
RANBAXY |
None (Tentative Approval) |
Lamivudine, Zidovudine, Nevirapine Tabs 150mg/300mg/200mg |
021939 |
001 |
NDA |
LAMIVUDINE; ZIDOVUDINE; NEVIRAPINE |
TABLET; ORAL |
150MG; 300MG; 200MG |
No
|
No
|
2006/06/30
(TA)
|
--
|
AUROBINDO PHARMA LTD |
None (Tentative Approval) |
LAMIVUDINE; STAVUDINE; NEVIRAPINE |
021969 |
001 |
NDA |
LAMIVUDINE; STAVUDINE; NEVIRAPINE |
TABLET; ORAL |
150MG; 30MG; 200MG |
No
|
No
|
2006/11/17
(TA)
|
--
|
CIPLA LIMITED |
None (Tentative Approval) |
LAMIVUDINE; STAVUDINE; NEVIRAPINE |
021969 |
002 |
NDA |
LAMIVUDINE; STAVUDINE; NEVIRAPINE |
TABLET; ORAL |
150MG; 40MG; 200MG |
No
|
No
|
2006/11/17
(TA)
|
--
|
CIPLA LIMITED |
None (Tentative Approval) |
LAMIVUDINE; ZIDOVUDINE; NEVIRAPINE |
021971 |
001 |
NDA |
LAMIVUDINE; ZIDOVUDINE; NEVIRAPINE |
TABLET; ORAL |
150MG; 300MG; 200MG |
No
|
No
|
2007/01/31
(TA)
|
--
|
CIPLA LIMITED |
None (Tentative Approval) |
Lamivudine/Zidovudine 150 mg/300 mg Tablets Co-packaged with Nevirapine 200 mg Tablets |
021988 |
001 |
NDA |
LAMIVUDINE; ZIDOVUDINE; NEVIRAPINE |
TABLET; ORAL |
150MG; 300MG; 200MG |
No
|
No
|
2007/03/02
(TA)
|
--
|
STRIDES ACROLAB |
None (Tentative Approval) |
STAVUDINE; LAMIVUDINE W/NEVIRAPINE |
021854 |
001 |
NDA |
STAVUDINE; LAMIVUDINE; NEVIRAPINE |
TABLET; ORAL |
40MG; 150MG; 200MG |
No
|
No
|
2007/03/13
(TA)
|
--
|
STRIDES ACROLAB |
None (Tentative Approval) |
NEVIRAPINE |
078887 |
001 |
ANDA |
NEVIRAPINE |
TABLET; ORAL |
200MG |
No
|
No
|
2007/09/28
(TA)
|
--
|
EMCURE PHARMA |
None (Tentative Approval) |
STAVUDINE; LAMIVUDINE; NEVIRAPINE |
021837 |
001 |
NDA |
STAVUDINE; LAMIVUDINE; NEVIRAPINE |
TABLET; ORAL |
40MG; 150MG; 200MG |
No
|
No
|
2008/03/20
(TA)
|
--
|
STRIDES ARCOLAB |
None (Tentative Approval) |
STAVUDINE; LAMIVUDINE; NEVIRAPINE |
022177 |
001 |
NDA |
STAVUDINE; LAMIVUDINE; NEVIRAPINE |
TABLET; ORAL |
30MG; 150MG; 200MG |
No
|
No
|
2008/03/20
(TA)
|
--
|
STRIDES ACROLAB |
None (Tentative Approval) |
LAMIVUDINE; NEVIRAPINE; ZIDOVUDINE |
022061 |
001 |
NDA |
LAMIVUDINE; NEVIRAPINE; ZIDOVUDINE |
TABLET; ORAL |
150MG; 200MG; 300MG |
No
|
No
|
2008/10/21
(TA)
|
--
|
MATRIX LABS |
None (Tentative Approval) |
STAVUDINE; LAMIVUDINE; NEVIRAPINE |
022346 |
001 |
NDA |
STAVUDINE; LAMIVUDINE; NEVIRAPINE |
TABLET; ORAL |
30MG; 150MG; 200MG |
No
|
No
|
2009/02/27
(TA)
|
--
|
PHARMACARE LTD |
None (Tentative Approval) |
STAVUDINE; LAMIVUDINE; NEVIRAPINE |
022346 |
002 |
NDA |
STAVUDINE; LAMIVUDINE; NEVIRAPINE |
TABLET; ORAL |
40MG; 150MG; 200MG |
No
|
No
|
2009/02/27
(TA)
|
--
|
PHARMACARE LTD |
None (Tentative Approval) |
LAMIVUDINE, ZIDOVUDINE TABS 150MG/300MG CO-PACKAGED WITH NEVIRAPINE TABS 200MG |
022356 |
001 |
NDA |
LAMIVUDINE; ZIDOVUDINE; NEVIRAPINE |
TABLET; ORAL |
150MG; 300MG; 200MG |
No
|
No
|
2009/05/07
(TA)
|
--
|
HETERO DRUGS LTD |
None (Tentative Approval) |
STAVUDINE; LAMIVUDINE; NEVIRAPINE |
022342 |
001 |
NDA |
STAVUDINE; LAMIVUDINE; NEVIRAPINE |
TABLET; ORAL |
30MG; 150MG; 200MG |
No
|
No
|
2009/07/16
(TA)
|
--
|
EMCURE PHARMA |
None (Tentative Approval) |
STAVUDINE; LAMIVUDINE; NEVIRAPINE |
022342 |
002 |
NDA |
STAVUDINE; LAMIVUDINE; NEVIRAPINE |
TABLET; ORAL |
40MG; 150MG; 200MG |
No
|
No
|
2009/07/16
(TA)
|
--
|
EMCURE PHARMA |
None (Tentative Approval) |
LAMIVUDINE; NEVIRAPINE; ZIDOVUDINE |
022464 |
001 |
NDA |
LAMIVUDINE; NEVIRAPINE; ZIDOVUDINE |
TABLET; ORAL |
150MG; 200MG; 300MG |
No
|
No
|
2009/12/22
(TA)
|
--
|
STRIDES ARCOLAB LTD |
None (Tentative Approval) |
NEVIRAPINE TABLETS FOR ORAL SUSPENSION |
022299 |
001 |
NDA |
NEVIRAPINE |
TABLET; ORAL |
50MG |
No
|
No
|
2010/02/24
(TA)
|
--
|
AUROBINDO PHARMA LTD |
None (Tentative Approval) |
LAMIVUDINE/NEVIRAPINE/ZIDOVUDINE TABLETS |
200793 |
001 |
NDA |
Lamivudine; Nevirapine; Zidovudine |
TABLET, FOR SUSPENSION; ORAL |
30MG; 50MG; 60MG |
No
|
No
|
2010/07/08
(TA)
|
--
|
MATRIX LABS |
None (Tentative Approval) |
LAMIVUDINE, NEVIRAPINE, AND STAVUDINE |
022537 |
001 |
NDA |
LAMIVUDINE, NEVIRAPINE, AND STAVUDINE |
TABLET; ORAL |
150MG;200MG;30MG |
No
|
No
|
2010/08/30
(TA)
|
--
|
MACLEODS PHARMA |
None (Tentative Approval) |