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
71335-1341-8	71335-1341	HUMAN PRESCRIPTION DRUG	Valacyclovir Hydrochloride	Valacyclovir Hydrochloride	TABLET, FILM COATED	ORAL	20211228	N/A	ANDA	ANDA078518	Bryant Ranch Prepack	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1341-8)
71335-1341-9	71335-1341	HUMAN PRESCRIPTION DRUG	Valacyclovir Hydrochloride	Valacyclovir Hydrochloride	TABLET, FILM COATED	ORAL	20200204	N/A	ANDA	ANDA078518	Bryant Ranch Prepack	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (71335-1341-9)
82868-055-21	82868-055	HUMAN PRESCRIPTION DRUG	Valacyclovir Hydrochloride	valacyclovir	TABLET, FILM COATED	ORAL	20240530	N/A	ANDA	ANDA078518	Northwind Health Company, LLC	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-055-21)
68788-8482-3	68788-8482	HUMAN PRESCRIPTION DRUG	Valacyclovir Hydrochloride	valacyclovir	TABLET, FILM COATED	ORAL	20230714	N/A	ANDA	ANDA078518	Preferred Pharmaceuticals Inc.	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8482-3)
68788-8482-9	68788-8482	HUMAN PRESCRIPTION DRUG	Valacyclovir Hydrochloride	valacyclovir	TABLET, FILM COATED	ORAL	20230714	N/A	ANDA	ANDA078518	Preferred Pharmaceuticals Inc.	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8482-9)