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
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)
68071-2279-8	68071-2279	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20201015	N/A	ANDA	ANDA074891	NuCare Pharmaceuticals,Inc.	ACYCLOVIR	400 mg/1	15 TABLET in 1 BOTTLE (68071-2279-8)
60687-856-65	60687-856	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20260204	N/A	ANDA	ANDA074891	American Health Packaging	ACYCLOVIR	400 mg/1	50 BLISTER PACK in 1 CARTON (60687-856-65) / 1 TABLET in 1 BLISTER PACK (60687-856-11)
60687-856-01	60687-856	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20250324	N/A	ANDA	ANDA074891	American Health Packaging	ACYCLOVIR	400 mg/1	100 BLISTER PACK in 1 CARTON (60687-856-01) / 1 TABLET in 1 BLISTER PACK (60687-856-11)
60687-867-01	60687-867	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20250606	N/A	ANDA	ANDA074891	American Health Packaging	ACYCLOVIR	800 mg/1	100 BLISTER PACK in 1 CARTON (60687-867-01) / 1 TABLET in 1 BLISTER PACK (60687-867-11)
71205-371-35	71205-371	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20220208	N/A	ANDA	ANDA074891	Proficient Rx LP	ACYCLOVIR	400 mg/1	35 TABLET in 1 BOTTLE (71205-371-35)
71205-371-60	71205-371	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20220208	N/A	ANDA	ANDA074891	Proficient Rx LP	ACYCLOVIR	400 mg/1	60 TABLET in 1 BOTTLE (71205-371-60)
71205-371-90	71205-371	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20220208	N/A	ANDA	ANDA074891	Proficient Rx LP	ACYCLOVIR	400 mg/1	90 TABLET in 1 BOTTLE (71205-371-90)
71205-371-30	71205-371	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20220208	N/A	ANDA	ANDA074891	Proficient Rx LP	ACYCLOVIR	400 mg/1	30 TABLET in 1 BOTTLE (71205-371-30)
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)
71335-1645-0	71335-1645	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20200709	N/A	ANDA	ANDA074891	Bryant Ranch Prepack	ACYCLOVIR	400 mg/1	120 TABLET in 1 BOTTLE (71335-1645-0)
71335-1645-4	71335-1645	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20220128	N/A	ANDA	ANDA074891	Bryant Ranch Prepack	ACYCLOVIR	400 mg/1	50 TABLET in 1 BOTTLE (71335-1645-4)
71335-1645-5	71335-1645	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20220128	N/A	ANDA	ANDA074891	Bryant Ranch Prepack	ACYCLOVIR	400 mg/1	15 TABLET in 1 BOTTLE (71335-1645-5)
71335-1645-6	71335-1645	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20200923	N/A	ANDA	ANDA074891	Bryant Ranch Prepack	ACYCLOVIR	400 mg/1	60 TABLET in 1 BOTTLE (71335-1645-6)
71335-1645-7	71335-1645	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20201218	N/A	ANDA	ANDA074891	Bryant Ranch Prepack	ACYCLOVIR	400 mg/1	25 TABLET in 1 BOTTLE (71335-1645-7)
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)