美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）
检索条件:" 注册申请号=ANDA076048"
符合检索条件的记录共 55 条，共 3 页，当前第 2 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
63187-061-60 63187-061 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20190101 20270131 ANDA ANDA076048 Proficient Rx LP OMEPRAZOLE 10 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-061-60)
63187-061-72 63187-061 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20190101 20270131 ANDA ANDA076048 Proficient Rx LP OMEPRAZOLE 10 mg/1 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-061-72)
63187-061-78 63187-061 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20190101 20270131 ANDA ANDA076048 Proficient Rx LP OMEPRAZOLE 10 mg/1 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-061-78)
63187-061-90 63187-061 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20190101 20270131 ANDA ANDA076048 Proficient Rx LP OMEPRAZOLE 10 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-061-90)
63187-070-14 63187-070 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20181101 20270131 ANDA ANDA076048 Proficient Rx LP OMEPRAZOLE 20 mg/1 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-070-14)
63187-070-30 63187-070 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20181101 20270131 ANDA ANDA076048 Proficient Rx LP OMEPRAZOLE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-070-30)
63187-070-60 63187-070 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20181101 20270131 ANDA ANDA076048 Proficient Rx LP OMEPRAZOLE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-070-60)
63187-070-72 63187-070 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20181101 20270131 ANDA ANDA076048 Proficient Rx LP OMEPRAZOLE 20 mg/1 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-070-72)
63187-070-78 63187-070 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20181101 20270131 ANDA ANDA076048 Proficient Rx LP OMEPRAZOLE 20 mg/1 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-070-78)
63187-070-90 63187-070 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20181101 20270131 ANDA ANDA076048 Proficient Rx LP OMEPRAZOLE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-070-90)
63187-170-30 63187-170 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20190101 20270131 ANDA ANDA076048 Proficient Rx LP OMEPRAZOLE 40 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-170-30)
63187-170-60 63187-170 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20190101 20270131 ANDA ANDA076048 Proficient Rx LP OMEPRAZOLE 40 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-170-60)
63187-170-90 63187-170 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20190101 20270131 ANDA ANDA076048 Proficient Rx LP OMEPRAZOLE 40 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-170-90)
60505-0065-0 60505-0065 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20031111 20260331 ANDA ANDA076048 Apotex Corp OMEPRAZOLE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (60505-0065-0)
60505-0065-1 60505-0065 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20031111 20270131 ANDA ANDA076048 Apotex Corp OMEPRAZOLE 20 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (60505-0065-1)
60505-0065-2 60505-0065 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20031111 20270131 ANDA ANDA076048 Apotex Corp OMEPRAZOLE 20 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (60505-0065-2)
60505-0145-0 60505-0145 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20031111 20260331 ANDA ANDA076048 Apotex Corp OMEPRAZOLE 10 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (60505-0145-0)
60505-0145-2 60505-0145 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20031111 20270131 ANDA ANDA076048 Apotex Corp OMEPRAZOLE 10 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (60505-0145-2)
60505-0146-0 60505-0146 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20090121 20260331 ANDA ANDA076048 Apotex Corp OMEPRAZOLE 40 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (60505-0146-0)
60505-0146-1 60505-0146 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20090121 20270131 ANDA ANDA076048 Apotex Corp OMEPRAZOLE 40 mg/1 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (60505-0146-1)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase