| 60760-698-60 |
60760-698 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20250513 |
N/A |
ANDA |
ANDA090554 |
ST. MARY'S MEDICAL PARK PHARMACY |
DIVALPROEX SODIUM |
250 mg/1 |
60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-698-60) |
| 68084-782-61 |
68084-782 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20160126 |
20260630 |
ANDA |
ANDA090554 |
American Health Packaging |
DIVALPROEX SODIUM |
500 mg/1 |
90 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-782-61) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (68084-782-11) |
| 65862-959-01 |
65862-959 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20141024 |
N/A |
ANDA |
ANDA090554 |
Aurobindo Pharma Limited |
DIVALPROEX SODIUM |
125 mg/1 |
100 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-959-01) |
| 65862-959-05 |
65862-959 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20141024 |
N/A |
ANDA |
ANDA090554 |
Aurobindo Pharma Limited |
DIVALPROEX SODIUM |
125 mg/1 |
500 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-959-05) |
| 65862-959-10 |
65862-959 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20141024 |
N/A |
ANDA |
ANDA090554 |
Aurobindo Pharma Limited |
DIVALPROEX SODIUM |
125 mg/1 |
10 BLISTER PACK in 1 CARTON (65862-959-10) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
| 65862-959-71 |
65862-959 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20141024 |
N/A |
ANDA |
ANDA090554 |
Aurobindo Pharma Limited |
DIVALPROEX SODIUM |
125 mg/1 |
7000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-959-71) |
| 65862-959-99 |
65862-959 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20141024 |
N/A |
ANDA |
ANDA090554 |
Aurobindo Pharma Limited |
DIVALPROEX SODIUM |
125 mg/1 |
1000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-959-99) |
| 55154-4679-0 |
55154-4679 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20160126 |
20260630 |
ANDA |
ANDA090554 |
Cardinal Health 107, LLC |
DIVALPROEX SODIUM |
500 mg/1 |
10 BLISTER PACK in 1 BAG (55154-4679-0) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
| 71335-2158-1 |
71335-2158 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20220811 |
N/A |
ANDA |
ANDA090554 |
Bryant Ranch Prepack |
DIVALPROEX SODIUM |
500 mg/1 |
60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-1) |
| 71335-2158-2 |
71335-2158 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20230302 |
N/A |
ANDA |
ANDA090554 |
Bryant Ranch Prepack |
DIVALPROEX SODIUM |
500 mg/1 |
30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-2) |
| 71335-2158-3 |
71335-2158 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20220811 |
N/A |
ANDA |
ANDA090554 |
Bryant Ranch Prepack |
DIVALPROEX SODIUM |
500 mg/1 |
90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-3) |
| 71335-2158-4 |
71335-2158 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20240906 |
N/A |
ANDA |
ANDA090554 |
Bryant Ranch Prepack |
DIVALPROEX SODIUM |
500 mg/1 |
180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-4) |
| 71335-2158-5 |
71335-2158 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20220920 |
N/A |
ANDA |
ANDA090554 |
Bryant Ranch Prepack |
DIVALPROEX SODIUM |
500 mg/1 |
120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-5) |
| 70518-2357-0 |
70518-2357 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20191010 |
N/A |
ANDA |
ANDA090554 |
REMEDYREPACK INC. |
DIVALPROEX SODIUM |
500 mg/1 |
30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2357-0) |
| 70518-2357-1 |
70518-2357 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20210316 |
N/A |
ANDA |
ANDA090554 |
REMEDYREPACK INC. |
DIVALPROEX SODIUM |
500 mg/1 |
100 POUCH in 1 BOX (70518-2357-1) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-2357-2) |
| 70518-2357-5 |
70518-2357 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20220809 |
N/A |
ANDA |
ANDA090554 |
REMEDYREPACK INC. |
DIVALPROEX SODIUM |
500 mg/1 |
30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2357-5) |
| 55154-7145-0 |
55154-7145 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20150302 |
20260630 |
ANDA |
ANDA090554 |
Cardinal Health 107, LLC |
DIVALPROEX SODIUM |
250 mg/1 |
10 BLISTER PACK in 1 BAG (55154-7145-0) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
| 68084-776-01 |
68084-776 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20150302 |
20260630 |
ANDA |
ANDA090554 |
American Health Packaging |
DIVALPROEX SODIUM |
250 mg/1 |
100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-776-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (68084-776-11) |
| 65862-403-01 |
65862-403 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20141024 |
N/A |
ANDA |
ANDA090554 |
Aurobindo Pharma Limited |
DIVALPROEX SODIUM |
500 mg/1 |
100 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-403-01) |
| 65862-403-05 |
65862-403 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20141024 |
N/A |
ANDA |
ANDA090554 |
Aurobindo Pharma Limited |
DIVALPROEX SODIUM |
500 mg/1 |
500 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-403-05) |