| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71335-1756-4 | 71335-1756 | HUMAN PRESCRIPTION DRUG | FENOFIBRATE | FENOFIBRATE | TABLET | ORAL | 20211220 | N/A | ANDA | ANDA213864 | Bryant Ranch Prepack | FENOFIBRATE | 160 mg/1 | 28 TABLET in 1 BOTTLE (71335-1756-4) |
| 71335-1756-5 | 71335-1756 | HUMAN PRESCRIPTION DRUG | FENOFIBRATE | FENOFIBRATE | TABLET | ORAL | 20211220 | N/A | ANDA | ANDA213864 | Bryant Ranch Prepack | FENOFIBRATE | 160 mg/1 | 100 TABLET in 1 BOTTLE (71335-1756-5) |
| 50090-7927-0 | 50090-7927 | HUMAN PRESCRIPTION DRUG | FENOFIBRATE | FENOFIBRATE | TABLET | ORAL | 20260305 | N/A | ANDA | ANDA213864 | A-S Medication Solutions | FENOFIBRATE | 160 mg/1 | 90 TABLET in 1 BOTTLE (50090-7927-0) |
| 70756-215-51 | 70756-215 | HUMAN PRESCRIPTION DRUG | FENOFIBRATE | FENOFIBRATE | TABLET | ORAL | 20200910 | N/A | ANDA | ANDA213864 | Lifestar Pharma LLC | FENOFIBRATE | 160 mg/1 | 500 TABLET in 1 BOTTLE (70756-215-51) |
| 70756-215-90 | 70756-215 | HUMAN PRESCRIPTION DRUG | FENOFIBRATE | FENOFIBRATE | TABLET | ORAL | 20200910 | N/A | ANDA | ANDA213864 | Lifestar Pharma LLC | FENOFIBRATE | 160 mg/1 | 90 TABLET in 1 BOTTLE (70756-215-90) |