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
72162-1724-0	72162-1724	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20240812	20261231	ANDA	ANDA077309	Bryant Ranch Prepack	ACYCLOVIR	800 mg/1	40 TABLET in 1 BOTTLE (72162-1724-0)
72162-1724-1	72162-1724	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20240812	20261231	ANDA	ANDA077309	Bryant Ranch Prepack	ACYCLOVIR	800 mg/1	21 TABLET in 1 BOTTLE (72162-1724-1)
72162-1724-2	72162-1724	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20240812	20261231	ANDA	ANDA077309	Bryant Ranch Prepack	ACYCLOVIR	800 mg/1	25 TABLET in 1 BOTTLE (72162-1724-2)
72162-1724-3	72162-1724	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20240812	20261231	ANDA	ANDA077309	Bryant Ranch Prepack	ACYCLOVIR	800 mg/1	30 TABLET in 1 BOTTLE (72162-1724-3)
72162-1724-4	72162-1724	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20240812	20261231	ANDA	ANDA077309	Bryant Ranch Prepack	ACYCLOVIR	800 mg/1	35 TABLET in 1 BOTTLE (72162-1724-4)
72162-1724-5	72162-1724	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20240812	20261231	ANDA	ANDA077309	Bryant Ranch Prepack	ACYCLOVIR	800 mg/1	500 TABLET in 1 BOTTLE (72162-1724-5)
72162-1724-6	72162-1724	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20240812	20261231	ANDA	ANDA077309	Bryant Ranch Prepack	ACYCLOVIR	800 mg/1	60 TABLET in 1 BOTTLE (72162-1724-6)
70518-0427-1	70518-0427	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20170421	20261231	ANDA	ANDA077309	REMEDYREPACK INC.	ACYCLOVIR	400 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (70518-0427-1)
70518-0427-3	70518-0427	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20210920	20261231	ANDA	ANDA077309	REMEDYREPACK INC.	ACYCLOVIR	400 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (70518-0427-3)
70518-0427-4	70518-0427	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20240521	20261231	ANDA	ANDA077309	REMEDYREPACK INC.	ACYCLOVIR	400 mg/1	28 TABLET in 1 BOTTLE, PLASTIC (70518-0427-4)
0904-5790-61	0904-5790	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20070209	20251231	ANDA	ANDA077309	Major Pharmaceuticals	ACYCLOVIR	400 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-5790-61) / 1 TABLET in 1 BLISTER PACK
68071-2247-1	68071-2247	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20200824	20261231	ANDA	ANDA077309	NuCare Pharmaceuticals,Inc.	ACYCLOVIR	400 mg/1	100 TABLET in 1 BOTTLE (68071-2247-1)
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)
68071-2287-4	68071-2287	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20201027	20261231	ANDA	ANDA077309	NuCare Pharmaceuticals,Inc.	ACYCLOVIR	400 mg/1	4 TABLET in 1 BOTTLE (68071-2287-4)
68071-5100-3	68071-5100	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20060313	20261231	ANDA	ANDA077309	NuCare Pharmaceuticals,Inc.	ACYCLOVIR	800 mg/1	30 TABLET in 1 BOTTLE (68071-5100-3)
63187-192-30	63187-192	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20190101	N/A	ANDA	ANDA077309	Proficient Rx LP	ACYCLOVIR	800 mg/1	30 TABLET in 1 BOTTLE (63187-192-30)
63187-192-35	63187-192	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20190101	N/A	ANDA	ANDA077309	Proficient Rx LP	ACYCLOVIR	800 mg/1	35 TABLET in 1 BOTTLE (63187-192-35)
63187-192-60	63187-192	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20190101	N/A	ANDA	ANDA077309	Proficient Rx LP	ACYCLOVIR	800 mg/1	60 TABLET in 1 BOTTLE (63187-192-60)
63187-192-90	63187-192	HUMAN PRESCRIPTION DRUG	acyclovir	acyclovir	TABLET	ORAL	20190101	N/A	ANDA	ANDA077309	Proficient Rx LP	ACYCLOVIR	800 mg/1	90 TABLET in 1 BOTTLE (63187-192-90)