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=ANDA074069"
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
71610-124-09 71610-124 HUMAN PRESCRIPTION DRUG AZATHIOPRINE Azathioprine TABLET ORAL 20180817 N/A ANDA ANDA074069 Aphena Pharma Solutions - Tennessee, LLC AZATHIOPRINE 50 mg/1 9000 TABLET in 1 BOTTLE (71610-124-09)
60219-1076-1 60219-1076 HUMAN PRESCRIPTION DRUG AZATHIOPRINE Azathioprine TABLET ORAL 20150202 N/A ANDA ANDA074069 Amneal Pharmaceuticals NY LLC AZATHIOPRINE 50 mg/1 100 TABLET in 1 BOTTLE (60219-1076-1)
42291-071-01 42291-071 HUMAN PRESCRIPTION DRUG AZATHIOPRINE Azathioprine TABLET ORAL 20220104 N/A ANDA ANDA074069 AvKARE AZATHIOPRINE 50 mg/1 100 TABLET in 1 BOTTLE (42291-071-01)
42291-063-01 42291-063 HUMAN PRESCRIPTION DRUG AZATHIOPRINE Azathioprine TABLET ORAL 20230413 N/A ANDA ANDA074069 AvKARE AZATHIOPRINE 100 mg/1 100 TABLET in 1 BOTTLE (42291-063-01)
69238-1076-1 69238-1076 HUMAN PRESCRIPTION DRUG AZATHIOPRINE Azathioprine TABLET ORAL 20150202 N/A ANDA ANDA074069 Amneal Pharmaceuticals NY LLC AZATHIOPRINE 50 mg/1 100 TABLET in 1 BOTTLE (69238-1076-1)
60219-2036-1 60219-2036 HUMAN PRESCRIPTION DRUG AZATHIOPRINE Azathioprine TABLET ORAL 20211108 N/A ANDA ANDA074069 Amneal Pharmaceuticals NY LLC AZATHIOPRINE 75 mg/1 100 TABLET in 1 BOTTLE (60219-2036-1)
60219-2037-1 60219-2037 HUMAN PRESCRIPTION DRUG AZATHIOPRINE Azathioprine TABLET ORAL 20211108 N/A ANDA ANDA074069 Amneal Pharmaceuticals NY LLC AZATHIOPRINE 100 mg/1 100 TABLET in 1 BOTTLE (60219-2037-1)
72789-129-30 72789-129 HUMAN PRESCRIPTION DRUG AZATHIOPRINE Azathioprine TABLET ORAL 20201008 N/A ANDA ANDA074069 PD-Rx Pharmaceuticals, Inc. AZATHIOPRINE 50 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (72789-129-30)
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