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
60505-5306-1	60505-5306	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20070609	20261231	ANDA	ANDA077309	Apotex Corp.	ACYCLOVIR	400 mg/1	100 TABLET in 1 BOTTLE (60505-5306-1)
60505-5306-8	60505-5306	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20070609	20251231	ANDA	ANDA077309	Apotex Corp.	ACYCLOVIR	400 mg/1	1000 TABLET in 1 BOTTLE (60505-5306-8)
60505-5307-1	60505-5307	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20060313	20261231	ANDA	ANDA077309	Apotex Corp.	ACYCLOVIR	800 mg/1	100 TABLET in 1 BOTTLE (60505-5307-1)
60505-5307-5	60505-5307	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20060313	20251231	ANDA	ANDA077309	Apotex Corp.	ACYCLOVIR	800 mg/1	500 TABLET in 1 BOTTLE (60505-5307-5)
71205-391-25	71205-391	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20200128	N/A	ANDA	ANDA077309	Proficient Rx LP	ACYCLOVIR	400 mg/1	25 TABLET in 1 BOTTLE (71205-391-25)
71205-391-30	71205-391	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20200128	N/A	ANDA	ANDA077309	Proficient Rx LP	ACYCLOVIR	400 mg/1	30 TABLET in 1 BOTTLE (71205-391-30)
71205-391-60	71205-391	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20200128	N/A	ANDA	ANDA077309	Proficient Rx LP	ACYCLOVIR	400 mg/1	60 TABLET in 1 BOTTLE (71205-391-60)
71205-391-90	71205-391	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20200128	N/A	ANDA	ANDA077309	Proficient Rx LP	ACYCLOVIR	400 mg/1	90 TABLET in 1 BOTTLE (71205-391-90)
61919-003-30	61919-003	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20140101	N/A	ANDA	ANDA077309	DIRECT RX	ACYCLOVIR	800 mg/1	30 TABLET in 1 BOTTLE (61919-003-30)
61919-003-35	61919-003	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20140101	N/A	ANDA	ANDA077309	DIRECT RX	ACYCLOVIR	800 mg/1	35 TABLET in 1 BOTTLE (61919-003-35)
71335-1381-0	71335-1381	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20240709	20261231	ANDA	ANDA077309	Bryant Ranch Prepack	ACYCLOVIR	800 mg/1	500 TABLET in 1 BOTTLE (71335-1381-0)
71335-1381-1	71335-1381	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20240709	20261231	ANDA	ANDA077309	Bryant Ranch Prepack	ACYCLOVIR	800 mg/1	25 TABLET in 1 BOTTLE (71335-1381-1)
71335-1381-2	71335-1381	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20191031	20261231	ANDA	ANDA077309	Bryant Ranch Prepack	ACYCLOVIR	800 mg/1	35 TABLET in 1 BOTTLE (71335-1381-2)
71335-1381-3	71335-1381	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20191028	20261231	ANDA	ANDA077309	Bryant Ranch Prepack	ACYCLOVIR	800 mg/1	30 TABLET in 1 BOTTLE (71335-1381-3)
71335-1381-4	71335-1381	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20240709	20261231	ANDA	ANDA077309	Bryant Ranch Prepack	ACYCLOVIR	800 mg/1	60 TABLET in 1 BOTTLE (71335-1381-4)
71335-1381-5	71335-1381	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20240709	20261231	ANDA	ANDA077309	Bryant Ranch Prepack	ACYCLOVIR	800 mg/1	50 TABLET in 1 BOTTLE (71335-1381-5)
71335-1381-6	71335-1381	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20240709	20261231	ANDA	ANDA077309	Bryant Ranch Prepack	ACYCLOVIR	800 mg/1	10 TABLET in 1 BOTTLE (71335-1381-6)
71335-1381-7	71335-1381	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20240709	20261231	ANDA	ANDA077309	Bryant Ranch Prepack	ACYCLOVIR	800 mg/1	40 TABLET in 1 BOTTLE (71335-1381-7)
71335-1381-8	71335-1381	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20200519	20261231	ANDA	ANDA077309	Bryant Ranch Prepack	ACYCLOVIR	800 mg/1	21 TABLET in 1 BOTTLE (71335-1381-8)
71335-1381-9	71335-1381	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20240709	20261231	ANDA	ANDA077309	Bryant Ranch Prepack	ACYCLOVIR	800 mg/1	90 TABLET in 1 BOTTLE (71335-1381-9)