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
31722-778-01	31722-778	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20131129	N/A	ANDA	ANDA203834	Camber Pharmaceuticals, Inc.	ACYCLOVIR	800 mg/1	100 TABLET in 1 BOTTLE (31722-778-01)
31722-778-05	31722-778	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20131129	N/A	ANDA	ANDA203834	Camber Pharmaceuticals, Inc.	ACYCLOVIR	800 mg/1	500 TABLET in 1 BOTTLE (31722-778-05)
51655-679-35	51655-679	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20230302	N/A	ANDA	ANDA203834	Northwind Health Company, LLC	ACYCLOVIR	800 mg/1	35 TABLET in 1 BOTTLE, PLASTIC (51655-679-35)
51655-679-51	51655-679	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20230215	N/A	ANDA	ANDA203834	Northwind Health Company, LLC	ACYCLOVIR	800 mg/1	40 TABLET in 1 BOTTLE, PLASTIC (51655-679-51)
51655-679-52	51655-679	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20230602	N/A	ANDA	ANDA203834	Northwind Health Company, LLC	ACYCLOVIR	800 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-679-52)