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
71335-2555-3	71335-2555	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20250123	N/A	ANDA	ANDA209366	Bryant Ranch Prepack	ACYCLOVIR	800 mg/1	30 TABLET in 1 BOTTLE (71335-2555-3)
71335-2555-4	71335-2555	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20250123	N/A	ANDA	ANDA209366	Bryant Ranch Prepack	ACYCLOVIR	800 mg/1	60 TABLET in 1 BOTTLE (71335-2555-4)
71335-2555-5	71335-2555	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20250123	N/A	ANDA	ANDA209366	Bryant Ranch Prepack	ACYCLOVIR	800 mg/1	50 TABLET in 1 BOTTLE (71335-2555-5)
71335-2555-6	71335-2555	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20250123	N/A	ANDA	ANDA209366	Bryant Ranch Prepack	ACYCLOVIR	800 mg/1	10 TABLET in 1 BOTTLE (71335-2555-6)
68071-3573-4	68071-3573	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20240215	N/A	ANDA	ANDA209366	NuCare Pharmaceuticals,Inc.	ACYCLOVIR	400 mg/1	4 TABLET in 1 BOTTLE (68071-3573-4)
71335-2555-0	71335-2555	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20250123	N/A	ANDA	ANDA209366	Bryant Ranch Prepack	ACYCLOVIR	800 mg/1	500 TABLET in 1 BOTTLE (71335-2555-0)
71335-2555-7	71335-2555	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20250123	N/A	ANDA	ANDA209366	Bryant Ranch Prepack	ACYCLOVIR	800 mg/1	40 TABLET in 1 BOTTLE (71335-2555-7)
71335-2555-8	71335-2555	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20250123	N/A	ANDA	ANDA209366	Bryant Ranch Prepack	ACYCLOVIR	800 mg/1	21 TABLET in 1 BOTTLE (71335-2555-8)
71335-2555-9	71335-2555	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20250123	N/A	ANDA	ANDA209366	Bryant Ranch Prepack	ACYCLOVIR	800 mg/1	90 TABLET in 1 BOTTLE (71335-2555-9)