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=ANDA206606"
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
70771-1081-6 70771-1081 HUMAN PRESCRIPTION DRUG acyclovir ACYCLOVIR INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20170817 N/A ANDA ANDA206606 Zydus Lifesciences Limited ACYCLOVIR SODIUM 500 mg/1 10 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (70771-1081-6)
70771-1082-6 70771-1082 HUMAN PRESCRIPTION DRUG acyclovir ACYCLOVIR INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20170817 N/A ANDA ANDA206606 Zydus Lifesciences Limited ACYCLOVIR SODIUM 1000 mg/1 10 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (70771-1082-6)
68382-125-10 68382-125 HUMAN PRESCRIPTION DRUG acyclovir ACYCLOVIR INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20170817 N/A ANDA ANDA206606 Zydus Pharmaceuticals USA Inc. ACYCLOVIR SODIUM 500 mg/1 10 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (68382-125-10)
68382-126-10 68382-126 HUMAN PRESCRIPTION DRUG acyclovir ACYCLOVIR INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20170817 N/A ANDA ANDA206606 Zydus Pharmaceuticals USA Inc. ACYCLOVIR SODIUM 1000 mg/1 10 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (68382-126-10)
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