| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71093-142-04 | 71093-142 | HUMAN PRESCRIPTION DRUG | CLOPIDOGREL BISULFATE | clopidogrel bisulfate | TABLET, FILM COATED | ORAL | 20220701 | N/A | ANDA | ANDA078004 | ACI Healthcare USA, Inc | CLOPIDOGREL BISULFATE | 75 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (71093-142-04) |
| 71093-142-05 | 71093-142 | HUMAN PRESCRIPTION DRUG | CLOPIDOGREL BISULFATE | clopidogrel bisulfate | TABLET, FILM COATED | ORAL | 20220701 | N/A | ANDA | ANDA078004 | ACI Healthcare USA, Inc | CLOPIDOGREL BISULFATE | 75 mg/1 | 500 TABLET, FILM COATED in 1 BOTTLE (71093-142-05) |