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
71335-1757-1	71335-1757	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20220128	N/A	ANDA	ANDA074891	Bryant Ranch Prepack	ACYCLOVIR	400 mg/1	35 TABLET in 1 BOTTLE (71335-1757-1)
71335-1757-2	71335-1757	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20210104	N/A	ANDA	ANDA074891	Bryant Ranch Prepack	ACYCLOVIR	400 mg/1	90 TABLET in 1 BOTTLE (71335-1757-2)
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)
71205-371-35	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)
70518-2085-1	70518-2085	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20230409	N/A	ANDA	ANDA074891	REMEDYREPACK INC.	ACYCLOVIR	400 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (70518-2085-1)
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)
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)
23155-227-01	23155-227	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20130808	N/A	ANDA	ANDA074891	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	ACYCLOVIR	400 mg/1	100 TABLET in 1 BOTTLE (23155-227-01)
23155-227-05	23155-227	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20130808	N/A	ANDA	ANDA074891	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	ACYCLOVIR	400 mg/1	500 TABLET in 1 BOTTLE (23155-227-05)
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)
23155-228-01	23155-228	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20130808	N/A	ANDA	ANDA074891	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	ACYCLOVIR	800 mg/1	100 TABLET in 1 BOTTLE (23155-228-01)
23155-228-05	23155-228	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20130808	N/A	ANDA	ANDA074891	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	ACYCLOVIR	800 mg/1	500 TABLET in 1 BOTTLE (23155-228-05)
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)
71335-1645-1	71335-1645	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20200702	N/A	ANDA	ANDA074891	Bryant Ranch Prepack	ACYCLOVIR	400 mg/1	20 TABLET in 1 BOTTLE (71335-1645-1)
71335-1645-2	71335-1645	HUMAN PRESCRIPTION DRUG	ACYCLOVIR	ACYCLOVIR	TABLET	ORAL	20220128	N/A	ANDA	ANDA074891	Bryant Ranch Prepack	ACYCLOVIR	400 mg/1	28 TABLET in 1 BOTTLE (71335-1645-2)