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=ANDA212931"
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
43547-897-10 43547-897 HUMAN PRESCRIPTION DRUG Bumetanide Bumetanide TABLET ORAL 20250301 N/A ANDA ANDA212931 Solco Healthcare LLC BUMETANIDE 1 mg/1 100 TABLET in 1 BOTTLE (43547-897-10)
43547-897-50 43547-897 HUMAN PRESCRIPTION DRUG Bumetanide Bumetanide TABLET ORAL 20250301 N/A ANDA ANDA212931 Solco Healthcare LLC BUMETANIDE 1 mg/1 500 TABLET in 1 BOTTLE (43547-897-50)
43547-896-10 43547-896 HUMAN PRESCRIPTION DRUG Bumetanide Bumetanide TABLET ORAL 20250301 N/A ANDA ANDA212931 Solco Healthcare LLC BUMETANIDE .5 mg/1 100 TABLET in 1 BOTTLE (43547-896-10)
43547-898-10 43547-898 HUMAN PRESCRIPTION DRUG Bumetanide Bumetanide TABLET ORAL 20250301 N/A ANDA ANDA212931 Solco Healthcare LLC BUMETANIDE 2 mg/1 100 TABLET in 1 BOTTLE (43547-898-10)
43547-898-50 43547-898 HUMAN PRESCRIPTION DRUG Bumetanide Bumetanide TABLET ORAL 20250301 N/A ANDA ANDA212931 Solco Healthcare LLC BUMETANIDE 2 mg/1 500 TABLET in 1 BOTTLE (43547-898-50)
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