71610-249-30 |
71610-249 |
HUMAN PRESCRIPTION DRUG |
Divalproex sodium |
Divalproex sodium |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20200915 |
N/A |
ANDA |
ANDA202419 |
Aphena Pharma Solutions - Tennessee, LLC |
DIVALPROEX SODIUM |
500 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-249-30) |
71610-249-53 |
71610-249 |
HUMAN PRESCRIPTION DRUG |
Divalproex sodium |
Divalproex sodium |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20190314 |
N/A |
ANDA |
ANDA202419 |
Aphena Pharma Solutions - Tennessee, LLC |
DIVALPROEX SODIUM |
500 mg/1 |
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-249-53) |
71610-249-60 |
71610-249 |
HUMAN PRESCRIPTION DRUG |
Divalproex sodium |
Divalproex sodium |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20190314 |
N/A |
ANDA |
ANDA202419 |
Aphena Pharma Solutions - Tennessee, LLC |
DIVALPROEX SODIUM |
500 mg/1 |
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-249-60) |
71610-249-80 |
71610-249 |
HUMAN PRESCRIPTION DRUG |
Divalproex sodium |
Divalproex sodium |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20201009 |
N/A |
ANDA |
ANDA202419 |
Aphena Pharma Solutions - Tennessee, LLC |
DIVALPROEX SODIUM |
500 mg/1 |
180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-249-80) |
71610-249-70 |
71610-249 |
HUMAN PRESCRIPTION DRUG |
Divalproex sodium |
Divalproex sodium |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20190314 |
N/A |
ANDA |
ANDA202419 |
Aphena Pharma Solutions - Tennessee, LLC |
DIVALPROEX SODIUM |
500 mg/1 |
120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-249-70) |
16714-485-01 |
16714-485 |
HUMAN PRESCRIPTION DRUG |
Divalproex sodium |
Divalproex sodium |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20140602 |
N/A |
ANDA |
ANDA202419 |
NorthStar Rx LLC |
DIVALPROEX SODIUM |
500 mg/1 |
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16714-485-01) |
16714-484-01 |
16714-484 |
HUMAN PRESCRIPTION DRUG |
Divalproex sodium |
Divalproex sodium |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20140602 |
N/A |
ANDA |
ANDA202419 |
NorthStar Rx LLC |
DIVALPROEX SODIUM |
250 mg/1 |
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16714-484-01) |
16714-484-02 |
16714-484 |
HUMAN PRESCRIPTION DRUG |
Divalproex sodium |
Divalproex sodium |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20140602 |
N/A |
ANDA |
ANDA202419 |
NorthStar Rx LLC |
DIVALPROEX SODIUM |
250 mg/1 |
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16714-484-02) |
16714-485-02 |
16714-485 |
HUMAN PRESCRIPTION DRUG |
Divalproex sodium |
Divalproex sodium |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20140602 |
N/A |
ANDA |
ANDA202419 |
NorthStar Rx LLC |
DIVALPROEX SODIUM |
500 mg/1 |
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16714-485-02) |
65862-594-01 |
65862-594 |
HUMAN PRESCRIPTION DRUG |
Divalproex sodium |
Divalproex sodium |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20140602 |
N/A |
ANDA |
ANDA202419 |
Aurobindo Pharma Limited |
DIVALPROEX SODIUM |
250 mg/1 |
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-01) |
65862-594-05 |
65862-594 |
HUMAN PRESCRIPTION DRUG |
Divalproex sodium |
Divalproex sodium |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20140602 |
N/A |
ANDA |
ANDA202419 |
Aurobindo Pharma Limited |
DIVALPROEX SODIUM |
250 mg/1 |
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-05) |
65862-595-01 |
65862-595 |
HUMAN PRESCRIPTION DRUG |
Divalproex sodium |
Divalproex sodium |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20140602 |
N/A |
ANDA |
ANDA202419 |
Aurobindo Pharma Limited |
DIVALPROEX SODIUM |
500 mg/1 |
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-595-01) |
65862-595-05 |
65862-595 |
HUMAN PRESCRIPTION DRUG |
Divalproex sodium |
Divalproex sodium |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20140602 |
N/A |
ANDA |
ANDA202419 |
Aurobindo Pharma Limited |
DIVALPROEX SODIUM |
500 mg/1 |
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-595-05) |
65862-595-10 |
65862-595 |
HUMAN PRESCRIPTION DRUG |
Divalproex sodium |
Divalproex sodium |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20140602 |
N/A |
ANDA |
ANDA202419 |
Aurobindo Pharma Limited |
DIVALPROEX SODIUM |
500 mg/1 |
10 BLISTER PACK in 1 CARTON (65862-595-10) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
65862-594-99 |
65862-594 |
HUMAN PRESCRIPTION DRUG |
Divalproex sodium |
Divalproex sodium |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20140602 |
N/A |
ANDA |
ANDA202419 |
Aurobindo Pharma Limited |
DIVALPROEX SODIUM |
250 mg/1 |
1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-99) |
71610-289-60 |
71610-289 |
HUMAN PRESCRIPTION DRUG |
Divalproex sodium |
Divalproex sodium |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20190605 |
N/A |
ANDA |
ANDA202419 |
Aphena Pharma Solutions - Tennessee, LLC |
DIVALPROEX SODIUM |
250 mg/1 |
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-289-60) |
71610-289-75 |
71610-289 |
HUMAN PRESCRIPTION DRUG |
Divalproex sodium |
Divalproex sodium |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20190605 |
N/A |
ANDA |
ANDA202419 |
Aphena Pharma Solutions - Tennessee, LLC |
DIVALPROEX SODIUM |
250 mg/1 |
150 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-289-75) |
65862-594-10 |
65862-594 |
HUMAN PRESCRIPTION DRUG |
Divalproex sodium |
Divalproex sodium |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20140602 |
N/A |
ANDA |
ANDA202419 |
Aurobindo Pharma Limited |
DIVALPROEX SODIUM |
250 mg/1 |
10 BLISTER PACK in 1 CARTON (65862-594-10) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
65862-594-60 |
65862-594 |
HUMAN PRESCRIPTION DRUG |
Divalproex sodium |
Divalproex sodium |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20140602 |
N/A |
ANDA |
ANDA202419 |
Aurobindo Pharma Limited |
DIVALPROEX SODIUM |
250 mg/1 |
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-60) |
71610-289-30 |
71610-289 |
HUMAN PRESCRIPTION DRUG |
Divalproex sodium |
Divalproex sodium |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20190605 |
N/A |
ANDA |
ANDA202419 |
Aphena Pharma Solutions - Tennessee, LLC |
DIVALPROEX SODIUM |
250 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-289-30) |