| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 72603-317-30 | 72603-317 | HUMAN PRESCRIPTION DRUG | PANTOPRAZOLE SODIUM | PANTOPRAZOLE SODIUM | GRANULE, DELAYED RELEASE | ORAL | 20241001 | N/A | ANDA | ANDA213725 | NorthStar RxLLC | PANTOPRAZOLE SODIUM | 40 mg/1 | 30 PACKET in 1 CARTON (72603-317-30) / 1 GRANULE, DELAYED RELEASE in 1 PACKET (72603-317-01) |
| 62756-071-64 | 62756-071 | HUMAN PRESCRIPTION DRUG | PANTOPRAZOLE SODIUM | PANTOPRAZOLE SODIUM | GRANULE, DELAYED RELEASE | ORAL | 20200701 | N/A | ANDA | ANDA213725 | Sun Pharmaceutical Industries, Inc. | PANTOPRAZOLE SODIUM | 40 mg/1 | 30 PACKET in 1 CARTON (62756-071-64) / 1 GRANULE, DELAYED RELEASE in 1 PACKET (62756-071-60) |