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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
24979-112-07 | 24979-112 | HUMAN PRESCRIPTION DRUG | Fenofibric Acid Delayed-Release | Fenofibric Acid | CAPSULE, DELAYED RELEASE | ORAL | 20200601 | N/A | ANDA | ANDA210469 | TWi Pharmaceuticals, Inc. | CHOLINE FENOFIBRATE | 135 mg/1 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (24979-112-07) |
24979-109-07 | 24979-109 | HUMAN PRESCRIPTION DRUG | Fenofibric Acid Delayed-Release | Fenofibric Acid | CAPSULE, DELAYED RELEASE | ORAL | 20200601 | N/A | ANDA | ANDA210469 | TWi Pharmaceuticals, Inc. | CHOLINE FENOFIBRATE | 45 mg/1 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (24979-109-07) |