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
0173-0565-04	0173-0565	HUMAN PRESCRIPTION DRUG	VALTREX	valacyclovir hydrochloride	TABLET, FILM COATED	ORAL	20020812	N/A	NDA	NDA020487	GlaxoSmithKline LLC	VALACYCLOVIR HYDROCHLORIDE	1 g/1	30 TABLET, FILM COATED in 1 BOTTLE (0173-0565-04)
0173-0565-10	0173-0565	HUMAN PRESCRIPTION DRUG	VALTREX	valacyclovir hydrochloride	TABLET, FILM COATED	ORAL	20020812	N/A	NDA	NDA020487	GlaxoSmithKline LLC	VALACYCLOVIR HYDROCHLORIDE	1 g/1	90 TABLET, FILM COATED in 1 BOTTLE (0173-0565-10)
0173-0933-08	0173-0933	HUMAN PRESCRIPTION DRUG	VALTREX	valacyclovir hydrochloride	TABLET, FILM COATED	ORAL	19950801	N/A	NDA	NDA020487	GlaxoSmithKline LLC	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0173-0933-08)
0173-0933-10	0173-0933	HUMAN PRESCRIPTION DRUG	VALTREX	valacyclovir hydrochloride	TABLET, FILM COATED	ORAL	19950801	N/A	NDA	NDA020487	GlaxoSmithKline LLC	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (0173-0933-10)
70518-2039-1	70518-2039	HUMAN PRESCRIPTION DRUG	VALTREX	valacyclovir hydrochloride	TABLET, FILM COATED	ORAL	20230717	N/A	NDA	NDA020487	REMEDYREPACK INC.	VALACYCLOVIR HYDROCHLORIDE	1 g/1	14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2039-1)
70518-2039-2	70518-2039	HUMAN PRESCRIPTION DRUG	VALTREX	valacyclovir hydrochloride	TABLET, FILM COATED	ORAL	20231002	N/A	NDA	NDA020487	REMEDYREPACK INC.	VALACYCLOVIR HYDROCHLORIDE	1 g/1	5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2039-2)