| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71335-1429-3 | 71335-1429 | HUMAN PRESCRIPTION DRUG | Pantoprazole Sodium | pantoprazole sodium | TABLET, DELAYED RELEASE | ORAL | 20200120 | N/A | ANDA | ANDA090970 | Bryant Ranch Prepack | PANTOPRAZOLE SODIUM | 40 mg/1 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1429-3) |
| 71335-1429-4 | 71335-1429 | HUMAN PRESCRIPTION DRUG | Pantoprazole Sodium | pantoprazole sodium | TABLET, DELAYED RELEASE | ORAL | 20240520 | N/A | ANDA | ANDA090970 | Bryant Ranch Prepack | PANTOPRAZOLE SODIUM | 40 mg/1 | 58 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1429-4) |
| 51079-051-20 | 51079-051 | HUMAN PRESCRIPTION DRUG | Pantoprazole Sodium | pantoprazole sodium | TABLET, DELAYED RELEASE | ORAL | 20110223 | N/A | ANDA | ANDA090970 | Mylan Institutional Inc. | PANTOPRAZOLE SODIUM | 40 mg/1 | 100 BLISTER PACK in 1 CARTON (51079-051-20) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (51079-051-01) |