| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 63187-042-90 | 63187-042 | HUMAN PRESCRIPTION DRUG | Pantoprazole Sodium | Pantoprazole Sodium | TABLET, DELAYED RELEASE | ORAL | 20181101 | N/A | ANDA | ANDA090797 | Proficient Rx LP | PANTOPRAZOLE SODIUM | 20 mg/1 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-042-90) |
| 63187-042-60 | 63187-042 | HUMAN PRESCRIPTION DRUG | Pantoprazole Sodium | Pantoprazole Sodium | TABLET, DELAYED RELEASE | ORAL | 20181101 | N/A | ANDA | ANDA090797 | Proficient Rx LP | PANTOPRAZOLE SODIUM | 20 mg/1 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-042-60) |
| 63187-042-30 | 63187-042 | HUMAN PRESCRIPTION DRUG | Pantoprazole Sodium | Pantoprazole Sodium | TABLET, DELAYED RELEASE | ORAL | 20181101 | N/A | ANDA | ANDA090797 | Proficient Rx LP | PANTOPRAZOLE SODIUM | 20 mg/1 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-042-30) |