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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
50090-6142-1 | 50090-6142 | HUMAN PRESCRIPTION DRUG | KETOCONAZOLE | ketoconazole | TABLET | ORAL | 20221003 | N/A | ANDA | ANDA075912 | A-S Medication Solutions | KETOCONAZOLE | 200 mg/1 | 7 TABLET in 1 BOTTLE (50090-6142-1) |
35573-433-30 | 35573-433 | HUMAN PRESCRIPTION DRUG | KETOCONAZOLE | ketoconazole | TABLET | ORAL | 20200410 | N/A | ANDA | ANDA075912 | Burel Pharmaceuticals, LLC | KETOCONAZOLE | 200 mg/1 | 30 TABLET in 1 BOTTLE (35573-433-30) |
35573-433-02 | 35573-433 | HUMAN PRESCRIPTION DRUG | KETOCONAZOLE | ketoconazole | TABLET | ORAL | 20200410 | N/A | ANDA | ANDA075912 | Burel Pharmaceuticals, LLC | KETOCONAZOLE | 200 mg/1 | 100 TABLET in 1 BOTTLE (35573-433-02) |
72189-180-07 | 72189-180 | HUMAN PRESCRIPTION DRUG | KETOCONAZOLE | KETOCONAZOLE | TABLET | ORAL | 20210224 | N/A | ANDA | ANDA075912 | Direct Rx | KETOCONAZOLE | 200 mg/1 | 7 TABLET in 1 BOTTLE (72189-180-07) |