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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
70748-258-07 | 70748-258 | HUMAN PRESCRIPTION DRUG | POSACONAZOLE | POSACONAZOLE | TABLET, DELAYED RELEASE | ORAL | 20210217 | N/A | ANDA | ANDA213454 | Lupin Pharmaceuticals, Inc. | POSACONAZOLE | 100 mg/1 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (70748-258-07) |
0904-7149-10 | 0904-7149 | HUMAN PRESCRIPTION DRUG | POSACONAZOLE | POSACONAZOLE | TABLET, DELAYED RELEASE | ORAL | 20210203 | N/A | ANDA | ANDA213454 | Major Pharmaceuticals | POSACONAZOLE | 100 mg/1 | 20 BLISTER PACK in 1 CARTON (0904-7149-10) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
0904-7149-04 | 0904-7149 | HUMAN PRESCRIPTION DRUG | POSACONAZOLE | POSACONAZOLE | TABLET, DELAYED RELEASE | ORAL | 20210203 | N/A | ANDA | ANDA213454 | Major Pharmaceuticals | POSACONAZOLE | 100 mg/1 | 30 BLISTER PACK in 1 CARTON (0904-7149-04) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK |