| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 72162-2152-9 | 72162-2152 | HUMAN PRESCRIPTION DRUG | Fenofibrate | fenofibrate | TABLET, FILM COATED | ORAL | 20231207 | N/A | ANDA | ANDA076520 | Bryant Ranch Prepack | FENOFIBRATE | 160 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-2152-9) |
| 43353-898-19 | 43353-898 | HUMAN PRESCRIPTION DRUG | Fenofibrate | fenofibrate | TABLET, FILM COATED | ORAL | 20140306 | N/A | ANDA | ANDA076520 | Aphena Pharma Solutions - Tennessee, LLC | FENOFIBRATE | 160 mg/1 | 3060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43353-898-19) |