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=ANDA206535"
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
70771-1383-6 70771-1383 HUMAN PRESCRIPTION DRUG acyclovir ACYCLOVIR INJECTION, SOLUTION INTRAVENOUS 20181127 N/A ANDA ANDA206535 Zydus Lifesciences Limited ACYCLOVIR SODIUM 50 mg/mL 10 VIAL, SINGLE-USE in 1 CARTON (70771-1383-6) / 10 mL in 1 VIAL, SINGLE-USE (70771-1383-1)
70771-1384-6 70771-1384 HUMAN PRESCRIPTION DRUG acyclovir ACYCLOVIR INJECTION, SOLUTION INTRAVENOUS 20181127 N/A ANDA ANDA206535 Zydus Lifesciences Limited ACYCLOVIR SODIUM 50 mg/mL 10 VIAL, SINGLE-USE in 1 CARTON (70771-1384-6) / 20 mL in 1 VIAL, SINGLE-USE (70771-1384-1)
68382-049-10 68382-049 HUMAN PRESCRIPTION DRUG acyclovir ACYCLOVIR INJECTION, SOLUTION INTRAVENOUS 20181127 N/A ANDA ANDA206535 Zydus Pharmaceuticals (USA) Inc. ACYCLOVIR SODIUM 50 mg/mL 10 VIAL, SINGLE-USE in 1 CARTON (68382-049-10) / 20 mL in 1 VIAL, SINGLE-USE (68382-049-01)
68382-048-10 68382-048 HUMAN PRESCRIPTION DRUG acyclovir ACYCLOVIR INJECTION, SOLUTION INTRAVENOUS 20181127 N/A ANDA ANDA206535 Zydus Pharmaceuticals (USA) Inc. ACYCLOVIR SODIUM 50 mg/mL 10 VIAL, SINGLE-USE in 1 CARTON (68382-048-10) / 10 mL in 1 VIAL, SINGLE-USE (68382-048-01)
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