68001-472-00 |
68001-472 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20210120 |
N/A |
ANDA |
ANDA079163 |
BluePoint Laboratories |
DIVALPROEX SODIUM |
125 mg/1 |
100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-472-00) |
68001-472-03 |
68001-472 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20210120 |
N/A |
ANDA |
ANDA079163 |
BluePoint Laboratories |
DIVALPROEX SODIUM |
125 mg/1 |
500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-472-03) |
68001-473-00 |
68001-473 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20210120 |
N/A |
ANDA |
ANDA079163 |
BluePoint Laboratories |
DIVALPROEX SODIUM |
250 mg/1 |
100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-473-00) |
68001-473-03 |
68001-473 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20210120 |
N/A |
ANDA |
ANDA079163 |
BluePoint Laboratories |
DIVALPROEX SODIUM |
250 mg/1 |
500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-473-03) |
68001-474-00 |
68001-474 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20210120 |
N/A |
ANDA |
ANDA079163 |
BluePoint Laboratories |
DIVALPROEX SODIUM |
500 mg/1 |
100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-474-00) |
68001-474-03 |
68001-474 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20210120 |
N/A |
ANDA |
ANDA079163 |
BluePoint Laboratories |
DIVALPROEX SODIUM |
500 mg/1 |
500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-474-03) |
63187-742-30 |
63187-742 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20161003 |
N/A |
ANDA |
ANDA079163 |
Proficient Rx LP |
DIVALPROEX SODIUM |
250 mg/1 |
30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-742-30) |
63187-742-60 |
63187-742 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20161003 |
N/A |
ANDA |
ANDA079163 |
Proficient Rx LP |
DIVALPROEX SODIUM |
250 mg/1 |
60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-742-60) |
63187-742-90 |
63187-742 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20161003 |
N/A |
ANDA |
ANDA079163 |
Proficient Rx LP |
DIVALPROEX SODIUM |
250 mg/1 |
90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-742-90) |
63187-743-30 |
63187-743 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20161003 |
N/A |
ANDA |
ANDA079163 |
Proficient Rx LP |
DIVALPROEX SODIUM |
500 mg/1 |
30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-743-30) |
63187-743-60 |
63187-743 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20161003 |
N/A |
ANDA |
ANDA079163 |
Proficient Rx LP |
DIVALPROEX SODIUM |
500 mg/1 |
60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-743-60) |
63187-743-90 |
63187-743 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20161003 |
N/A |
ANDA |
ANDA079163 |
Proficient Rx LP |
DIVALPROEX SODIUM |
500 mg/1 |
90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-743-90) |
61919-249-60 |
61919-249 |
HUMAN PRESCRIPTION DRUG |
DIVALPROEX SODIUM |
divalproex sodium |
TABLET, DELAYED RELEASE |
ORAL |
20220406 |
N/A |
ANDA |
ANDA079163 |
DirectRx |
DIVALPROEX SODIUM |
500 mg/1 |
60 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-249-60) |
70518-2017-2 |
70518-2017 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20230130 |
N/A |
ANDA |
ANDA079163 |
REMEDYREPACK INC. |
DIVALPROEX SODIUM |
125 mg/1 |
30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2017-2) |
70934-948-60 |
70934-948 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20220203 |
20240531 |
ANDA |
ANDA079163 |
Denton Pharma, Inc. DBA Northwind Pharmaceuticals |
DIVALPROEX SODIUM |
500 mg/1 |
60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70934-948-60) |
70934-949-60 |
70934-949 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20220209 |
20240630 |
ANDA |
ANDA079163 |
Denton Pharma, Inc. DBA Northwind Pharmaceuticals |
DIVALPROEX SODIUM |
250 mg/1 |
60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70934-949-60) |
29300-138-01 |
29300-138 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20111001 |
N/A |
ANDA |
ANDA079163 |
Unichem Pharmaceuticals (USA), Inc. |
DIVALPROEX SODIUM |
125 mg/1 |
100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-138-01) |
29300-138-05 |
29300-138 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20111001 |
N/A |
ANDA |
ANDA079163 |
Unichem Pharmaceuticals (USA), Inc. |
DIVALPROEX SODIUM |
125 mg/1 |
500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-138-05) |
29300-138-10 |
29300-138 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20111001 |
N/A |
ANDA |
ANDA079163 |
Unichem Pharmaceuticals (USA), Inc. |
DIVALPROEX SODIUM |
125 mg/1 |
1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-138-10) |
29300-139-01 |
29300-139 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20111001 |
N/A |
ANDA |
ANDA079163 |
Unichem Pharmaceuticals (USA), Inc. |
DIVALPROEX SODIUM |
250 mg/1 |
100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-139-01) |