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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
67877-276-90 | 67877-276 | HUMAN PRESCRIPTION DRUG | CLOPIDOGREL | CLOPIDOGREL BISULFATE | TABLET | ORAL | 20240516 | N/A | ANDA | ANDA203632 | Ascend Laboratories, LLC | CLOPIDOGREL BISULFATE | 75 mg/1 | 90 TABLET in 1 BOTTLE (67877-276-90) |
67877-276-30 | 67877-276 | HUMAN PRESCRIPTION DRUG | CLOPIDOGREL | CLOPIDOGREL BISULFATE | TABLET | ORAL | 20240516 | N/A | ANDA | ANDA203632 | Ascend Laboratories, LLC | CLOPIDOGREL BISULFATE | 75 mg/1 | 30 TABLET in 1 BOTTLE (67877-276-30) |
67877-276-05 | 67877-276 | HUMAN PRESCRIPTION DRUG | CLOPIDOGREL | CLOPIDOGREL BISULFATE | TABLET | ORAL | 20240516 | N/A | ANDA | ANDA203632 | Ascend Laboratories, LLC | CLOPIDOGREL BISULFATE | 75 mg/1 | 500 TABLET in 1 BOTTLE (67877-276-05) |