| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0115-1522-10 | 0115-1522 | HUMAN PRESCRIPTION DRUG | Fenofibrate | Fenofibrate | TABLET | ORAL | 20150624 | 20250831 | NDA AUTHORIZED GENERIC | NDA022118 | Amneal Pharmaceuticals of New York LLC | FENOFIBRATE | 40 mg/1 | 90 TABLET in 1 BOTTLE (0115-1522-10) |
| 0115-1523-10 | 0115-1523 | HUMAN PRESCRIPTION DRUG | Fenofibrate | Fenofibrate | TABLET | ORAL | 20150624 | 20250831 | NDA AUTHORIZED GENERIC | NDA022118 | Amneal Pharmaceuticals of New York LLC | FENOFIBRATE | 120 mg/1 | 90 TABLET in 1 BOTTLE (0115-1523-10) |