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
71335-0630-8	71335-0630	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20180529	N/A	ANDA	ANDA203047	Bryant Ranch Prepack	VALACYCLOVIR HYDROCHLORIDE	1 g/1	8 TABLET, FILM COATED in 1 BOTTLE (71335-0630-8)
31722-704-05	31722-704	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20150525	N/A	ANDA	ANDA203047	Camber Pharmaceuticals, Inc.	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (31722-704-05)
31722-704-32	31722-704	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20150525	N/A	ANDA	ANDA203047	Camber Pharmaceuticals, Inc.	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	10 TABLET, FILM COATED in 1 BLISTER PACK (31722-704-32)
31722-704-60	31722-704	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20150525	N/A	ANDA	ANDA203047	Camber Pharmaceuticals, Inc.	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (31722-704-60)
31722-704-01	31722-704	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20150525	N/A	ANDA	ANDA203047	Camber Pharmaceuticals, Inc.	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (31722-704-01)
31722-704-30	31722-704	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20150525	N/A	ANDA	ANDA203047	Camber Pharmaceuticals, Inc.	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (31722-704-30)
31722-704-31	31722-704	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20150525	N/A	ANDA	ANDA203047	Camber Pharmaceuticals, Inc.	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	10 TABLET, FILM COATED in 1 BLISTER PACK (31722-704-31)