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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
0781-2234-01 | 0781-2234 | HUMAN PRESCRIPTION DRUG | Omeprazole | Omeprazole | CAPSULE, DELAYED RELEASE | ORAL | 20090121 | N/A | ANDA | ANDA076515 | Sandoz Inc | OMEPRAZOLE | 40 mg/1 | 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2234-01) |
0781-2234-10 | 0781-2234 | HUMAN PRESCRIPTION DRUG | Omeprazole | Omeprazole | CAPSULE, DELAYED RELEASE | ORAL | 20090121 | N/A | ANDA | ANDA076515 | Sandoz Inc | OMEPRAZOLE | 40 mg/1 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2234-10) |
0781-2234-31 | 0781-2234 | HUMAN PRESCRIPTION DRUG | Omeprazole | Omeprazole | CAPSULE, DELAYED RELEASE | ORAL | 20090121 | N/A | ANDA | ANDA076515 | Sandoz Inc | OMEPRAZOLE | 40 mg/1 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2234-31) |