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
71335-1645-8	71335-1645	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20201223	N/A	ANDA	ANDA074891	Bryant Ranch Prepack	ACYCLOVIR	400 mg/1	10 TABLET in 1 BOTTLE (71335-1645-8)
71335-1645-9	71335-1645	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20220128	N/A	ANDA	ANDA074891	Bryant Ranch Prepack	ACYCLOVIR	400 mg/1	40 TABLET in 1 BOTTLE (71335-1645-9)
71205-388-30	71205-388	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20220208	N/A	ANDA	ANDA074891	Proficient Rx LP	ACYCLOVIR	800 mg/1	30 TABLET in 1 BOTTLE (71205-388-30)
71205-388-35	71205-388	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20220208	N/A	ANDA	ANDA074891	Proficient Rx LP	ACYCLOVIR	800 mg/1	35 TABLET in 1 BOTTLE (71205-388-35)
71205-388-60	71205-388	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20220208	N/A	ANDA	ANDA074891	Proficient Rx LP	ACYCLOVIR	800 mg/1	60 TABLET in 1 BOTTLE (71205-388-60)
71205-388-90	71205-388	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20220208	N/A	ANDA	ANDA074891	Proficient Rx LP	ACYCLOVIR	800 mg/1	90 TABLET in 1 BOTTLE (71205-388-90)
70518-4186-0	70518-4186	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20240925	N/A	ANDA	ANDA074891	REMEDYREPACK INC.	ACYCLOVIR	800 mg/1	10 TABLET in 1 BOTTLE, PLASTIC (70518-4186-0)