| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 62175-118-43 | 62175-118 | HUMAN PRESCRIPTION DRUG | Omeprazole | omeprazole | CAPSULE, DELAYED RELEASE | ORAL | 20021104 | N/A | ANDA | ANDA075410 | Lannett Company, Inc. | OMEPRAZOLE | 20 mg/1 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-118-43) |
| 62175-118-46 | 62175-118 | HUMAN PRESCRIPTION DRUG | Omeprazole | omeprazole | CAPSULE, DELAYED RELEASE | ORAL | 20021104 | N/A | ANDA | ANDA075410 | Lannett Company, Inc. | OMEPRAZOLE | 20 mg/1 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-118-46) |
| 62175-118-49 | 62175-118 | HUMAN PRESCRIPTION DRUG | Omeprazole | omeprazole | CAPSULE, DELAYED RELEASE | ORAL | 20021104 | N/A | ANDA | ANDA075410 | Lannett Company, Inc. | OMEPRAZOLE | 20 mg/1 | 54000 CAPSULE, DELAYED RELEASE in 1 DRUM (62175-118-49) |