| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0781-2790-01 | 0781-2790 | HUMAN PRESCRIPTION DRUG | Omeprazole | Omeprazole | CAPSULE, DELAYED RELEASE | ORAL | 20030128 | N/A | ANDA | ANDA075757 | Sandoz Inc | OMEPRAZOLE | 20 mg/1 | 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2790-01) |
| 0781-2868-31 | 0781-2868 | HUMAN PRESCRIPTION DRUG | Omeprazole | Omeprazole | CAPSULE, DELAYED RELEASE | ORAL | 20190701 | N/A | ANDA | ANDA075757 | Sandoz Inc | OMEPRAZOLE | 20 mg/1 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2868-31) |
| 0781-2868-92 | 0781-2868 | HUMAN PRESCRIPTION DRUG | Omeprazole | Omeprazole | CAPSULE, DELAYED RELEASE | ORAL | 20190701 | N/A | ANDA | ANDA075757 | Sandoz Inc | OMEPRAZOLE | 20 mg/1 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2868-92) |