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
51407-107-30	51407-107	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20220627	N/A	ANDA	ANDA076588	Golden State Medical Supply, Inc.	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (51407-107-30)
51407-107-90	51407-107	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20220627	N/A	ANDA	ANDA076588	Golden State Medical Supply, Inc.	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (51407-107-90)
51407-108-30	51407-108	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20220627	N/A	ANDA	ANDA076588	Golden State Medical Supply, Inc.	VALACYCLOVIR HYDROCHLORIDE	1 g/1	30 TABLET, FILM COATED in 1 BOTTLE (51407-108-30)
51407-108-90	51407-108	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20220627	N/A	ANDA	ANDA076588	Golden State Medical Supply, Inc.	VALACYCLOVIR HYDROCHLORIDE	1 g/1	90 TABLET, FILM COATED in 1 BOTTLE (51407-108-90)
63304-904-03	63304-904	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20201219	N/A	ANDA	ANDA076588	SUN PHARMACEUTICAL INDUSTRIES, INC.	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (63304-904-03)
63304-904-05	63304-904	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20201219	N/A	ANDA	ANDA076588	SUN PHARMACEUTICAL INDUSTRIES, INC.	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (63304-904-05)
63304-904-30	63304-904	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20201219	N/A	ANDA	ANDA076588	SUN PHARMACEUTICAL INDUSTRIES, INC.	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63304-904-30)
63304-904-77	63304-904	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20201219	N/A	ANDA	ANDA076588	SUN PHARMACEUTICAL INDUSTRIES, INC.	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	100 BLISTER PACK in 1 CARTON (63304-904-77) / 1 TABLET, FILM COATED in 1 BLISTER PACK (63304-904-11)
63304-904-90	63304-904	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20201219	N/A	ANDA	ANDA076588	SUN PHARMACEUTICAL INDUSTRIES, INC.	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63304-904-90)
63304-905-03	63304-905	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20201219	N/A	ANDA	ANDA076588	SUN PHARMACEUTICAL INDUSTRIES, INC.	VALACYCLOVIR HYDROCHLORIDE	1 g/1	10 TABLET, FILM COATED in 1 BOTTLE (63304-905-03)
63304-905-05	63304-905	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20201219	N/A	ANDA	ANDA076588	SUN PHARMACEUTICAL INDUSTRIES, INC.	VALACYCLOVIR HYDROCHLORIDE	1 g/1	500 TABLET, FILM COATED in 1 BOTTLE (63304-905-05)
63304-905-30	63304-905	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20201219	N/A	ANDA	ANDA076588	SUN PHARMACEUTICAL INDUSTRIES, INC.	VALACYCLOVIR HYDROCHLORIDE	1 g/1	30 TABLET, FILM COATED in 1 BOTTLE (63304-905-30)
63304-905-77	63304-905	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20201219	N/A	ANDA	ANDA076588	SUN PHARMACEUTICAL INDUSTRIES, INC.	VALACYCLOVIR HYDROCHLORIDE	1 g/1	100 BLISTER PACK in 1 CARTON (63304-905-77) / 1 TABLET, FILM COATED in 1 BLISTER PACK (63304-905-11)
63304-905-90	63304-905	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20201219	N/A	ANDA	ANDA076588	SUN PHARMACEUTICAL INDUSTRIES, INC.	VALACYCLOVIR HYDROCHLORIDE	1 g/1	90 TABLET, FILM COATED in 1 BOTTLE (63304-905-90)