| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0008-0841-81 | 0008-0841 | HUMAN PRESCRIPTION DRUG | Protonix Delayed-Release | PANTOPRAZOLE SODIUM | TABLET, DELAYED RELEASE | ORAL | 20000501 | N/A | NDA | NDA020987 | Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | PANTOPRAZOLE SODIUM | 40 mg/1 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (0008-0841-81) |
| 0008-0843-81 | 0008-0843 | HUMAN PRESCRIPTION DRUG | Protonix Delayed-Release | PANTOPRAZOLE SODIUM | TABLET, DELAYED RELEASE | ORAL | 20000501 | N/A | NDA | NDA020987 | Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | PANTOPRAZOLE SODIUM | 20 mg/1 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (0008-0843-81) |