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=ANDA213057"
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
16714-008-01 16714-008 HUMAN PRESCRIPTION DRUG Isosorbide dinitrate Isosorbide dinitrate TABLET ORAL 20200501 N/A ANDA ANDA213057 Northstar Rx LLC ISOSORBIDE DINITRATE 10 mg/1 100 TABLET in 1 BOTTLE (16714-008-01)
70771-1501-0 70771-1501 HUMAN PRESCRIPTION DRUG Isosorbide dinitrate Isosorbide dinitrate TABLET ORAL 20191125 N/A ANDA ANDA213057 Zydus Lifesciences Limited ISOSORBIDE DINITRATE 5 mg/1 1000 TABLET in 1 BOTTLE (70771-1501-0)
70771-1501-1 70771-1501 HUMAN PRESCRIPTION DRUG Isosorbide dinitrate Isosorbide dinitrate TABLET ORAL 20191125 N/A ANDA ANDA213057 Zydus Lifesciences Limited ISOSORBIDE DINITRATE 5 mg/1 100 TABLET in 1 BOTTLE (70771-1501-1)
70771-1505-1 70771-1505 HUMAN PRESCRIPTION DRUG Isosorbide dinitrate Isosorbide dinitrate TABLET ORAL 20191125 N/A ANDA ANDA213057 Zydus Lifesciences Limited ISOSORBIDE DINITRATE 40 mg/1 100 TABLET in 1 BOTTLE (70771-1505-1)
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