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
57237-043-90	57237-043	HUMAN PRESCRIPTION DRUG	Valacyclovir Hydrochloride	Valacyclovir Hydrochloride	TABLET, FILM COATED	ORAL	20100524	N/A	ANDA	ANDA090682	Rising Pharma Holdings, Inc.	VALACYCLOVIR HYDROCHLORIDE	1 g/1	90 TABLET, FILM COATED in 1 BOTTLE (57237-043-90)
57237-042-90	57237-042	HUMAN PRESCRIPTION DRUG	Valacyclovir Hydrochloride	Valacyclovir Hydrochloride	TABLET, FILM COATED	ORAL	20100524	N/A	ANDA	ANDA090682	Rising Pharma Holdings, Inc.	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (57237-042-90)
57237-043-05	57237-043	HUMAN PRESCRIPTION DRUG	Valacyclovir Hydrochloride	Valacyclovir Hydrochloride	TABLET, FILM COATED	ORAL	20100524	N/A	ANDA	ANDA090682	Rising Pharma Holdings, Inc.	VALACYCLOVIR HYDROCHLORIDE	1 g/1	500 TABLET, FILM COATED in 1 BOTTLE (57237-043-05)
57237-042-05	57237-042	HUMAN PRESCRIPTION DRUG	Valacyclovir Hydrochloride	Valacyclovir Hydrochloride	TABLET, FILM COATED	ORAL	20100524	N/A	ANDA	ANDA090682	Rising Pharma Holdings, Inc.	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (57237-042-05)
68071-2738-1	68071-2738	HUMAN PRESCRIPTION DRUG	Valacyclovir Hydrochloride	Valacyclovir Hydrochloride	TABLET, FILM COATED	ORAL	20220527	N/A	ANDA	ANDA090682	NuCare Pharmaceuticals,Inc.	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (68071-2738-1)
68071-2738-4	68071-2738	HUMAN PRESCRIPTION DRUG	Valacyclovir Hydrochloride	Valacyclovir Hydrochloride	TABLET, FILM COATED	ORAL	20220527	N/A	ANDA	ANDA090682	NuCare Pharmaceuticals,Inc.	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (68071-2738-4)
68071-2749-3	68071-2749	HUMAN PRESCRIPTION DRUG	Valacyclovir Hydrochloride	Valacyclovir Hydrochloride	TABLET, FILM COATED	ORAL	20220602	N/A	ANDA	ANDA090682	NuCare Pharmaceuticals,Inc.	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-2749-3)
68071-2921-9	68071-2921	HUMAN PRESCRIPTION DRUG	Valacyclovir Hydrochloride	Valacyclovir Hydrochloride	TABLET, FILM COATED	ORAL	20230125	N/A	ANDA	ANDA090682	NuCare Pharmaceuticals,Inc.	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-2921-9)
70518-3359-0	70518-3359	HUMAN PRESCRIPTION DRUG	Valacyclovir Hydrochloride	Valacyclovir Hydrochloride	TABLET, FILM COATED	ORAL	20220207	N/A	ANDA	ANDA090682	REMEDYREPACK INC.	VALACYCLOVIR HYDROCHLORIDE	1 g/1	4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3359-0)
70518-3359-1	70518-3359	HUMAN PRESCRIPTION DRUG	Valacyclovir Hydrochloride	Valacyclovir Hydrochloride	TABLET, FILM COATED	ORAL	20220214	N/A	ANDA	ANDA090682	REMEDYREPACK INC.	VALACYCLOVIR HYDROCHLORIDE	1 g/1	21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3359-1)
71335-0708-2	71335-0708	HUMAN PRESCRIPTION DRUG	Valacyclovir Hydrochloride	Valacyclovir Hydrochloride	TABLET, FILM COATED	ORAL	20180412	N/A	ANDA	ANDA090682	Bryant Ranch Prepack	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71335-0708-2)
71335-0708-4	71335-0708	HUMAN PRESCRIPTION DRUG	Valacyclovir Hydrochloride	Valacyclovir Hydrochloride	TABLET, FILM COATED	ORAL	20180424	N/A	ANDA	ANDA090682	Bryant Ranch Prepack	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (71335-0708-4)
71335-0708-5	71335-0708	HUMAN PRESCRIPTION DRUG	Valacyclovir Hydrochloride	Valacyclovir Hydrochloride	TABLET, FILM COATED	ORAL	20211019	N/A	ANDA	ANDA090682	Bryant Ranch Prepack	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-0708-5)
71335-0708-6	71335-0708	HUMAN PRESCRIPTION DRUG	Valacyclovir Hydrochloride	Valacyclovir Hydrochloride	TABLET, FILM COATED	ORAL	20180226	N/A	ANDA	ANDA090682	Bryant Ranch Prepack	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0708-6)
71335-0708-7	71335-0708	HUMAN PRESCRIPTION DRUG	Valacyclovir Hydrochloride	Valacyclovir Hydrochloride	TABLET, FILM COATED	ORAL	20180816	N/A	ANDA	ANDA090682	Bryant Ranch Prepack	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	8 TABLET, FILM COATED in 1 BOTTLE (71335-0708-7)
71335-0708-8	71335-0708	HUMAN PRESCRIPTION DRUG	Valacyclovir Hydrochloride	Valacyclovir Hydrochloride	TABLET, FILM COATED	ORAL	20190614	N/A	ANDA	ANDA090682	Bryant Ranch Prepack	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0708-8)
71335-0708-9	71335-0708	HUMAN PRESCRIPTION DRUG	Valacyclovir Hydrochloride	Valacyclovir Hydrochloride	TABLET, FILM COATED	ORAL	20190422	N/A	ANDA	ANDA090682	Bryant Ranch Prepack	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (71335-0708-9)
71335-0708-3	71335-0708	HUMAN PRESCRIPTION DRUG	Valacyclovir Hydrochloride	Valacyclovir Hydrochloride	TABLET, FILM COATED	ORAL	20220420	N/A	ANDA	ANDA090682	Bryant Ranch Prepack	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	4 TABLET, FILM COATED in 1 BOTTLE (71335-0708-3)
71335-0708-0	71335-0708	HUMAN PRESCRIPTION DRUG	Valacyclovir Hydrochloride	Valacyclovir Hydrochloride	TABLET, FILM COATED	ORAL	20220210	N/A	ANDA	ANDA090682	Bryant Ranch Prepack	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0708-0)
71335-0708-1	71335-0708	HUMAN PRESCRIPTION DRUG	Valacyclovir Hydrochloride	Valacyclovir Hydrochloride	TABLET, FILM COATED	ORAL	20220111	N/A	ANDA	ANDA090682	Bryant Ranch Prepack	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-0708-1)