| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0115-1325-10 | 0115-1325 | HUMAN PRESCRIPTION DRUG | Fenofibric Acid | FENOFIBRIC ACID | CAPSULE, DELAYED RELEASE | ORAL | 20240601 | N/A | ANDA | ANDA200264 | Amneal Pharmaceuticals of New York LLC | FENOFIBRIC ACID | 135 mg/1 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0115-1325-10) |
| 0115-1324-10 | 0115-1324 | HUMAN PRESCRIPTION DRUG | Fenofibric Acid | FENOFIBRIC ACID | CAPSULE, DELAYED RELEASE | ORAL | 20240601 | N/A | ANDA | ANDA200264 | Amneal Pharmaceuticals of New York LLC | FENOFIBRIC ACID | 45 mg/1 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0115-1324-10) |