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）

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
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)
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)
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)
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)