| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71335-0291-6 | 71335-0291 | HUMAN PRESCRIPTION DRUG | Pantoprazole Sodium | Pantoprazole | TABLET, DELAYED RELEASE | ORAL | 20220628 | N/A | ANDA | ANDA205119 | Bryant Ranch Prepack | PANTOPRAZOLE SODIUM | 20 mg/1 | 10 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-6) |
| 71335-0291-7 | 71335-0291 | HUMAN PRESCRIPTION DRUG | Pantoprazole Sodium | Pantoprazole | TABLET, DELAYED RELEASE | ORAL | 20220628 | N/A | ANDA | ANDA205119 | Bryant Ranch Prepack | PANTOPRAZOLE SODIUM | 20 mg/1 | 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-7) |
| 71335-0291-8 | 71335-0291 | HUMAN PRESCRIPTION DRUG | Pantoprazole Sodium | Pantoprazole | TABLET, DELAYED RELEASE | ORAL | 20220628 | N/A | ANDA | ANDA205119 | Bryant Ranch Prepack | PANTOPRAZOLE SODIUM | 20 mg/1 | 180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-8) |