72789-353-01 |
72789-353 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20231018 |
N/A |
ANDA |
ANDA078597 |
PD-Rx Pharmaceuticals, Inc. |
DIVALPROEX SODIUM |
250 mg/1 |
100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-353-01) |
72789-354-01 |
72789-354 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20231017 |
N/A |
ANDA |
ANDA078597 |
PD-Rx Pharmaceuticals, Inc. |
DIVALPROEX SODIUM |
500 mg/1 |
100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-354-01) |
55154-4154-0 |
55154-4154 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20080729 |
N/A |
ANDA |
ANDA078597 |
Cardinal Health 107, LLC |
DIVALPROEX SODIUM |
250 mg/1 |
10 BLISTER PACK in 1 BAG (55154-4154-0) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
70518-2665-0 |
70518-2665 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20200330 |
N/A |
ANDA |
ANDA078597 |
REMEDYREPACK INC. |
DIVALPROEX SODIUM |
125 mg/1 |
30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2665-0) |
70518-2665-1 |
70518-2665 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20231031 |
N/A |
ANDA |
ANDA078597 |
REMEDYREPACK INC. |
DIVALPROEX SODIUM |
125 mg/1 |
100 POUCH in 1 BOX (70518-2665-1) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-2665-2) |
70518-2674-2 |
70518-2674 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20210430 |
N/A |
ANDA |
ANDA078597 |
REMEDYREPACK INC. |
DIVALPROEX SODIUM |
500 mg/1 |
30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2674-2) |
70518-2513-0 |
70518-2513 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20191230 |
N/A |
ANDA |
ANDA078597 |
REMEDYREPACK INC. |
DIVALPROEX SODIUM |
250 mg/1 |
100 POUCH in 1 BOX (70518-2513-0) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-2513-1) |
55154-2336-0 |
55154-2336 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20080729 |
N/A |
ANDA |
ANDA078597 |
Cardinal Health 107, LLC |
DIVALPROEX SODIUM |
500 mg/1 |
10 BLISTER PACK in 1 BAG (55154-2336-0) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
72162-2316-5 |
72162-2316 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20240516 |
N/A |
ANDA |
ANDA078597 |
Bryant Ranch Prepack |
DIVALPROEX SODIUM |
250 mg/1 |
500 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2316-5) |
72162-2316-1 |
72162-2316 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20240516 |
N/A |
ANDA |
ANDA078597 |
Bryant Ranch Prepack |
DIVALPROEX SODIUM |
250 mg/1 |
100 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2316-1) |
62756-796-18 |
62756-796 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20080729 |
N/A |
ANDA |
ANDA078597 |
Sun Pharmaceutical Industries, Inc. |
DIVALPROEX SODIUM |
125 mg/1 |
1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-796-18) |
62756-796-88 |
62756-796 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20080729 |
N/A |
ANDA |
ANDA078597 |
Sun Pharmaceutical Industries, Inc. |
DIVALPROEX SODIUM |
125 mg/1 |
100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-796-88) |
62756-797-08 |
62756-797 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20080729 |
N/A |
ANDA |
ANDA078597 |
Sun Pharmaceutical Industries, Inc. |
DIVALPROEX SODIUM |
250 mg/1 |
100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-08) |
62756-797-13 |
62756-797 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20080729 |
N/A |
ANDA |
ANDA078597 |
Sun Pharmaceutical Industries, Inc. |
DIVALPROEX SODIUM |
250 mg/1 |
500 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-13) |
62756-797-18 |
62756-797 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20080729 |
N/A |
ANDA |
ANDA078597 |
Sun Pharmaceutical Industries, Inc. |
DIVALPROEX SODIUM |
250 mg/1 |
1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-18) |
62756-797-83 |
62756-797 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20080729 |
N/A |
ANDA |
ANDA078597 |
Sun Pharmaceutical Industries, Inc. |
DIVALPROEX SODIUM |
250 mg/1 |
30 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-83) |
62756-797-88 |
62756-797 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20080729 |
N/A |
ANDA |
ANDA078597 |
Sun Pharmaceutical Industries, Inc. |
DIVALPROEX SODIUM |
250 mg/1 |
100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-88) |
62756-798-08 |
62756-798 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20080729 |
N/A |
ANDA |
ANDA078597 |
Sun Pharmaceutical Industries, Inc. |
DIVALPROEX SODIUM |
500 mg/1 |
100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-798-08) |
62756-796-83 |
62756-796 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20080729 |
N/A |
ANDA |
ANDA078597 |
Sun Pharmaceutical Industries, Inc. |
DIVALPROEX SODIUM |
125 mg/1 |
30 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-796-83) |
62756-796-08 |
62756-796 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20080729 |
N/A |
ANDA |
ANDA078597 |
Sun Pharmaceutical Industries, Inc. |
DIVALPROEX SODIUM |
125 mg/1 |
100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-796-08) |