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=ANDA211145"
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
70710-1128-5 70710-1128 HUMAN PRESCRIPTION DRUG Ursodiol Ursodiol TABLET ORAL 20181107 N/A ANDA ANDA211145 Zydus Pharmaceuticals (USA) Inc. URSODIOL 500 mg/1 500 TABLET in 1 BOTTLE (70710-1128-5)
70710-1128-1 70710-1128 HUMAN PRESCRIPTION DRUG Ursodiol Ursodiol TABLET ORAL 20181107 N/A ANDA ANDA211145 Zydus Pharmaceuticals (USA) Inc. URSODIOL 500 mg/1 100 TABLET in 1 BOTTLE (70710-1128-1)
70710-1127-5 70710-1127 HUMAN PRESCRIPTION DRUG Ursodiol Ursodiol TABLET ORAL 20181107 N/A ANDA ANDA211145 Zydus Pharmaceuticals (USA) Inc. URSODIOL 250 mg/1 500 TABLET in 1 BOTTLE (70710-1127-5)
70710-1127-1 70710-1127 HUMAN PRESCRIPTION DRUG Ursodiol Ursodiol TABLET ORAL 20181107 N/A ANDA ANDA211145 Zydus Pharmaceuticals (USA) Inc. URSODIOL 250 mg/1 100 TABLET in 1 BOTTLE (70710-1127-1)
70771-1407-1 70771-1407 HUMAN PRESCRIPTION DRUG Ursodiol Ursodiol TABLET ORAL 20181107 N/A ANDA ANDA211145 Zydus Lifesciences Limited URSODIOL 250 mg/1 100 TABLET in 1 BOTTLE (70771-1407-1)
70771-1407-5 70771-1407 HUMAN PRESCRIPTION DRUG Ursodiol Ursodiol TABLET ORAL 20181107 N/A ANDA ANDA211145 Zydus Lifesciences Limited URSODIOL 250 mg/1 500 TABLET in 1 BOTTLE (70771-1407-5)
70771-1408-1 70771-1408 HUMAN PRESCRIPTION DRUG Ursodiol Ursodiol TABLET ORAL 20181107 N/A ANDA ANDA211145 Zydus Lifesciences Limited URSODIOL 500 mg/1 100 TABLET in 1 BOTTLE (70771-1408-1)
70771-1408-5 70771-1408 HUMAN PRESCRIPTION DRUG Ursodiol Ursodiol TABLET ORAL 20181107 N/A ANDA ANDA211145 Zydus Lifesciences Limited URSODIOL 500 mg/1 500 TABLET in 1 BOTTLE (70771-1408-5)
60687-527-21 60687-527 HUMAN PRESCRIPTION DRUG Ursodiol Ursodiol TABLET ORAL 20200911 N/A ANDA ANDA211145 American Health Packaging URSODIOL 250 mg/1 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-527-21) / 1 TABLET in 1 BLISTER PACK (60687-527-11)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase