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=ANDA078295"
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
62756-520-18 62756-520 HUMAN PRESCRIPTION DRUG sumatriptan succinate sumatriptan succinate TABLET, FILM COATED ORAL 20090810 N/A ANDA ANDA078295 Sun Pharmaceutical Industries, Inc. SUMATRIPTAN SUCCINATE 25 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (62756-520-18)
72189-432-09 72189-432 HUMAN PRESCRIPTION DRUG Sumatriptan Succinate Sumatriptan Succinate TABLET, FILM COATED ORAL 20230313 N/A ANDA ANDA078295 Direct_Rx SUMATRIPTAN SUCCINATE 25 mg/1 9 TABLET, FILM COATED in 1 BOTTLE (72189-432-09)
72189-433-09 72189-433 HUMAN PRESCRIPTION DRUG Sumatriptan Succinate Sumatriptan Succinate TABLET, FILM COATED ORAL 20230313 N/A ANDA ANDA078295 Direct_Rx SUMATRIPTAN SUCCINATE 50 mg/1 9 TABLET, FILM COATED in 1 BOTTLE (72189-433-09)
62756-520-08 62756-520 HUMAN PRESCRIPTION DRUG sumatriptan succinate sumatriptan succinate TABLET, FILM COATED ORAL 20090810 N/A ANDA ANDA078295 Sun Pharmaceutical Industries, Inc. SUMATRIPTAN SUCCINATE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (62756-520-08)
62756-520-01 62756-520 HUMAN PRESCRIPTION DRUG sumatriptan succinate sumatriptan succinate TABLET, FILM COATED ORAL 20201101 N/A ANDA ANDA078295 Sun Pharmaceutical Industries, Inc. SUMATRIPTAN SUCCINATE 25 mg/1 3 BLISTER PACK in 1 CARTON (62756-520-01) / 9 TABLET, FILM COATED in 1 BLISTER PACK
50090-5939-0 50090-5939 HUMAN PRESCRIPTION DRUG sumatriptan succinate sumatriptan succinate TABLET, FILM COATED ORAL 20220311 N/A ANDA ANDA078295 A-S Medication Solutions SUMATRIPTAN SUCCINATE 25 mg/1 9 BLISTER PACK in 1 CARTON (50090-5939-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
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