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=ANDA077744"
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
0378-5630-59 0378-5630 HUMAN PRESCRIPTION DRUG Sumatriptan Succinate sumatriptan succinate TABLET, FILM COATED ORAL 20090810 N/A ANDA ANDA077744 Mylan Pharmaceuticals Inc. SUMATRIPTAN SUCCINATE 25 mg/1 9 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5630-59)
0378-5631-59 0378-5631 HUMAN PRESCRIPTION DRUG Sumatriptan Succinate sumatriptan succinate TABLET, FILM COATED ORAL 20090810 N/A ANDA ANDA077744 Mylan Pharmaceuticals Inc. SUMATRIPTAN SUCCINATE 50 mg/1 9 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5631-59)
0378-5632-59 0378-5632 HUMAN PRESCRIPTION DRUG Sumatriptan Succinate sumatriptan succinate TABLET, FILM COATED ORAL 20090810 N/A ANDA ANDA077744 Mylan Pharmaceuticals Inc. SUMATRIPTAN SUCCINATE 100 mg/1 9 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5632-59)
51407-011-09 51407-011 HUMAN PRESCRIPTION DRUG Sumatriptan Succinate sumatriptan succinate TABLET, FILM COATED ORAL 20180212 N/A ANDA ANDA077744 Golden State Medical Supply, Inc. SUMATRIPTAN SUCCINATE 25 mg/1 9 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51407-011-09)
51407-012-09 51407-012 HUMAN PRESCRIPTION DRUG Sumatriptan Succinate sumatriptan succinate TABLET, FILM COATED ORAL 20180212 N/A ANDA ANDA077744 Golden State Medical Supply, Inc. SUMATRIPTAN SUCCINATE 50 mg/1 9 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51407-012-09)
51407-013-09 51407-013 HUMAN PRESCRIPTION DRUG Sumatriptan Succinate sumatriptan succinate TABLET, FILM COATED ORAL 20180212 N/A ANDA ANDA077744 Golden State Medical Supply, Inc. SUMATRIPTAN SUCCINATE 100 mg/1 9 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51407-013-09)
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