| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0008-0844-02 | 0008-0844 | HUMAN PRESCRIPTION DRUG | Protonix Delayed-Release | PANTOPRAZOLE SODIUM | GRANULE, DELAYED RELEASE | ORAL | 20080229 | N/A | NDA | NDA022020 | Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | PANTOPRAZOLE SODIUM | 40 mg/1 | 30 PACKET in 1 CARTON (0008-0844-02) / 1 GRANULE, DELAYED RELEASE in 1 PACKET (0008-0844-01) |
| 55154-4232-0 | 55154-4232 | HUMAN PRESCRIPTION DRUG | Protonix Delayed-Release | pantoprazole sodium | GRANULE, DELAYED RELEASE | ORAL | 20080229 | N/A | NDA | NDA022020 | Cardinal Health 107, LLC | PANTOPRAZOLE SODIUM | 40 mg/1 | 10 PACKET in 1 BAG (55154-4232-0) / 40 GRANULE, DELAYED RELEASE in 1 PACKET |