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
71205-053-30	71205-053	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20180601	N/A	ANDA	ANDA075382	Proficient Rx LP	ACYCLOVIR	800 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (71205-053-30)
71205-056-30	71205-056	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20180601	N/A	ANDA	ANDA075382	Proficient Rx LP	ACYCLOVIR	400 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (71205-056-30)
71205-056-60	71205-056	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20180601	N/A	ANDA	ANDA075382	Proficient Rx LP	ACYCLOVIR	400 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (71205-056-60)
71205-056-90	71205-056	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20180601	N/A	ANDA	ANDA075382	Proficient Rx LP	ACYCLOVIR	400 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (71205-056-90)
71205-053-35	71205-053	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20180601	N/A	ANDA	ANDA075382	Proficient Rx LP	ACYCLOVIR	800 mg/1	35 TABLET in 1 BOTTLE, PLASTIC (71205-053-35)
71205-053-60	71205-053	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20180601	N/A	ANDA	ANDA075382	Proficient Rx LP	ACYCLOVIR	800 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (71205-053-60)
71205-053-90	71205-053	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20180601	N/A	ANDA	ANDA075382	Proficient Rx LP	ACYCLOVIR	800 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (71205-053-90)
50268-061-15	50268-061	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20110316	N/A	ANDA	ANDA075382	AvPAK	ACYCLOVIR	400 mg/1	50 BLISTER PACK in 1 BOTTLE, UNIT-DOSE (50268-061-15) / 1 TABLET in 1 BLISTER PACK (50268-061-11)
50268-062-15	50268-062	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20140718	N/A	ANDA	ANDA075382	AvPAK	ACYCLOVIR	800 mg/1	50 BLISTER PACK in 1 BOTTLE, UNIT-DOSE (50268-062-15) / 1 TABLET in 1 BLISTER PACK (50268-062-11)