| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 59651-575-90 | 59651-575 | HUMAN PRESCRIPTION DRUG | Fenofibrate | Fenofibrate | TABLET, FILM COATED | ORAL | 20220927 | N/A | ANDA | ANDA216798 | Aurobindo Pharma Limited | FENOFIBRATE | 54 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (59651-575-90) |
| 59651-576-90 | 59651-576 | HUMAN PRESCRIPTION DRUG | Fenofibrate | Fenofibrate | TABLET, FILM COATED | ORAL | 20220927 | N/A | ANDA | ANDA216798 | Aurobindo Pharma Limited | FENOFIBRATE | 160 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (59651-576-90) |
| 68071-3542-9 | 68071-3542 | HUMAN PRESCRIPTION DRUG | Fenofibrate | Fenofibrate | TABLET, FILM COATED | ORAL | 20231129 | N/A | ANDA | ANDA216798 | NuCare Pharmaceuticals,Inc. | FENOFIBRATE | 160 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-3542-9) |