| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0074-7325-13 | 0074-7325 | HUMAN PRESCRIPTION DRUG | Depakote | Divalproex Sodium | TABLET, DELAYED RELEASE | ORAL | 19830310 | N/A | NDA | NDA018723 | AbbVie Inc. | DIVALPROEX SODIUM | 125 mg/1 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (0074-7325-13) |
| 0074-7326-13 | 0074-7326 | HUMAN PRESCRIPTION DRUG | Depakote | Divalproex Sodium | TABLET, DELAYED RELEASE | ORAL | 20230630 | N/A | NDA | NDA018723 | AbbVie Inc. | DIVALPROEX SODIUM | 250 mg/1 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (0074-7326-13) |
| 0074-7327-13 | 0074-7327 | HUMAN PRESCRIPTION DRUG | Depakote | Divalproex Sodium | TABLET, DELAYED RELEASE | ORAL | 19830310 | N/A | NDA | NDA018723 | AbbVie Inc. | DIVALPROEX SODIUM | 500 mg/1 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (0074-7327-13) |
| 70518-3881-0 | 70518-3881 | HUMAN PRESCRIPTION DRUG | Depakote | Divalproex Sodium | TABLET, DELAYED RELEASE | ORAL | 20230926 | N/A | NDA | NDA018723 | REMEDYREPACK INC. | DIVALPROEX SODIUM | 125 mg/1 | 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3881-0) |