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=ANDA076847"
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
55111-291-98 55111-291 HUMAN PRESCRIPTION DRUG Sumatriptan Succinate Sumatriptan Succinate TABLET ORAL 20201210 N/A ANDA ANDA076847 Dr. Reddy's Laboratories Limited SUMATRIPTAN SUCCINATE 25 mg/1 3 BLISTER PACK in 1 CARTON (55111-291-98) / 9 TABLET in 1 BLISTER PACK
55111-291-01 55111-291 HUMAN PRESCRIPTION DRUG Sumatriptan Succinate Sumatriptan Succinate TABLET ORAL 20091117 N/A ANDA ANDA076847 Dr. Reddy's Laboratories Limited SUMATRIPTAN SUCCINATE 25 mg/1 100 TABLET in 1 BOTTLE (55111-291-01)
55111-291-05 55111-291 HUMAN PRESCRIPTION DRUG Sumatriptan Succinate Sumatriptan Succinate TABLET ORAL 20091117 N/A ANDA ANDA076847 Dr. Reddy's Laboratories Limited SUMATRIPTAN SUCCINATE 25 mg/1 500 TABLET in 1 BOTTLE (55111-291-05)
55111-291-09 55111-291 HUMAN PRESCRIPTION DRUG Sumatriptan Succinate Sumatriptan Succinate TABLET ORAL 20091117 N/A ANDA ANDA076847 Dr. Reddy's Laboratories Limited SUMATRIPTAN SUCCINATE 25 mg/1 9 BLISTER PACK in 1 CARTON (55111-291-09) / 1 TABLET in 1 BLISTER PACK
55111-291-30 55111-291 HUMAN PRESCRIPTION DRUG Sumatriptan Succinate Sumatriptan Succinate TABLET ORAL 20091117 N/A ANDA ANDA076847 Dr. Reddy's Laboratories Limited SUMATRIPTAN SUCCINATE 25 mg/1 30 TABLET in 1 BOTTLE (55111-291-30)
55111-291-36 55111-291 HUMAN PRESCRIPTION DRUG Sumatriptan Succinate Sumatriptan Succinate TABLET ORAL 20091117 N/A ANDA ANDA076847 Dr. Reddy's Laboratories Limited SUMATRIPTAN SUCCINATE 25 mg/1 36 TABLET in 1 BOTTLE (55111-291-36)
55111-291-90 55111-291 HUMAN PRESCRIPTION DRUG Sumatriptan Succinate Sumatriptan Succinate TABLET ORAL 20091117 N/A ANDA ANDA076847 Dr. Reddy's Laboratories Limited SUMATRIPTAN SUCCINATE 25 mg/1 90 TABLET in 1 BOTTLE (55111-291-90)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase