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=ANDA077070"
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
42806-122-10 42806-122 HUMAN PRESCRIPTION DRUG Sotalol Hydrochloride Sotalol Hydrochloride TABLET ORAL 20160104 N/A ANDA ANDA077070 Epic Pharma, LLC SOTALOL HYDROCHLORIDE 120 mg/1 1000 TABLET in 1 BOTTLE (42806-122-10)
42806-123-01 42806-123 HUMAN PRESCRIPTION DRUG Sotalol Hydrochloride Sotalol Hydrochloride TABLET ORAL 20160104 N/A ANDA ANDA077070 Epic Pharma, LLC SOTALOL HYDROCHLORIDE 160 mg/1 100 TABLET in 1 BOTTLE (42806-123-01)
42806-123-10 42806-123 HUMAN PRESCRIPTION DRUG Sotalol Hydrochloride Sotalol Hydrochloride TABLET ORAL 20160104 N/A ANDA ANDA077070 Epic Pharma, LLC SOTALOL HYDROCHLORIDE 160 mg/1 1000 TABLET in 1 BOTTLE (42806-123-10)
42806-122-01 42806-122 HUMAN PRESCRIPTION DRUG Sotalol Hydrochloride Sotalol Hydrochloride TABLET ORAL 20160104 N/A ANDA ANDA077070 Epic Pharma, LLC SOTALOL HYDROCHLORIDE 120 mg/1 100 TABLET in 1 BOTTLE (42806-122-01)
42806-121-10 42806-121 HUMAN PRESCRIPTION DRUG Sotalol Hydrochloride Sotalol Hydrochloride TABLET ORAL 20160104 N/A ANDA ANDA077070 Epic Pharma, LLC SOTALOL HYDROCHLORIDE 80 mg/1 1000 TABLET in 1 BOTTLE (42806-121-10)
42806-121-01 42806-121 HUMAN PRESCRIPTION DRUG Sotalol Hydrochloride Sotalol Hydrochloride TABLET ORAL 20160104 N/A ANDA ANDA077070 Epic Pharma, LLC SOTALOL HYDROCHLORIDE 80 mg/1 100 TABLET in 1 BOTTLE (42806-121-01)
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