| NDC包装代码 | 产品NDC | 产品类型 | 商品名 | 通用名 | 剂型 | 给药途径 | 上市日期 | 结束日期 | 市场类别 | 申请号 | 标签持有者 | 活性成分 | 规格 | 包装描述 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0074-3826-13 | 0074-3826 | HUMAN PRESCRIPTION DRUG | Depakote ER | Divalproex Sodium | TABLET, EXTENDED RELEASE | ORAL | 20000804 | 20240621 | NDA | NDA021168 | AbbVie Inc. | DIVALPROEX SODIUM | 250 mg/1 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0074-3826-13) |
| 0074-7401-13 | 0074-7401 | HUMAN PRESCRIPTION DRUG | Depakote ER | Divalproex Sodium | TABLET, EXTENDED RELEASE | ORAL | 20000804 | N/A | NDA | NDA021168 | AbbVie Inc. | DIVALPROEX SODIUM | 250 mg/1 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0074-7401-13) |
| 0074-7402-13 | 0074-7402 | HUMAN PRESCRIPTION DRUG | Depakote ER | Divalproex Sodium | TABLET, EXTENDED RELEASE | ORAL | 20000804 | N/A | NDA | NDA021168 | AbbVie Inc. | DIVALPROEX SODIUM | 500 mg/1 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0074-7402-13) |
| 70518-3754-0 | 70518-3754 | HUMAN PRESCRIPTION DRUG | Depakote ER | Divalproex Sodium | TABLET, EXTENDED RELEASE | ORAL | 20230608 | N/A | NDA | NDA021168 | REMEDYREPACK INC. | DIVALPROEX SODIUM | 250 mg/1 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3754-0) |