| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 69452-433-20 | 69452-433 | HUMAN PRESCRIPTION DRUG | divalproex sodium | divalproex sodium | TABLET, DELAYED RELEASE | ORAL | 20240626 | N/A | ANDA | ANDA078853 | Bionpharma Inc. | DIVALPROEX SODIUM | 125 mg/1 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-433-20) |
| 69452-433-30 | 69452-433 | HUMAN PRESCRIPTION DRUG | divalproex sodium | divalproex sodium | TABLET, DELAYED RELEASE | ORAL | 20240626 | N/A | ANDA | ANDA078853 | Bionpharma Inc. | DIVALPROEX SODIUM | 125 mg/1 | 500 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-433-30) |
| 50090-7763-0 | 50090-7763 | HUMAN PRESCRIPTION DRUG | divalproex sodium | divalproex sodium | TABLET, DELAYED RELEASE | ORAL | 20251111 | N/A | ANDA | ANDA078853 | A-S Medication Solutions | DIVALPROEX SODIUM | 250 mg/1 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7763-0) |
| 50090-7763-1 | 50090-7763 | HUMAN PRESCRIPTION DRUG | divalproex sodium | divalproex sodium | TABLET, DELAYED RELEASE | ORAL | 20251111 | N/A | ANDA | ANDA078853 | A-S Medication Solutions | DIVALPROEX SODIUM | 250 mg/1 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7763-1) |