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
65841-629-01	65841-629	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20180405	N/A	ANDA	ANDA079137	Zydus Lifesciences Limited	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65841-629-01)
65841-629-06	65841-629	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20180405	N/A	ANDA	ANDA079137	Zydus Lifesciences Limited	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65841-629-06)
65841-629-10	65841-629	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20180405	N/A	ANDA	ANDA079137	Zydus Lifesciences Limited	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65841-629-10)
65841-629-77	65841-629	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20180405	N/A	ANDA	ANDA079137	Zydus Lifesciences Limited	VALACYCLOVIR HYDROCHLORIDE	500 mg/1	10 BLISTER PACK in 1 CARTON (65841-629-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65841-629-30)
65841-630-06	65841-630	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20180405	N/A	ANDA	ANDA079137	Zydus Lifesciences Limited	VALACYCLOVIR HYDROCHLORIDE	1000 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65841-630-06)
65841-630-10	65841-630	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20180405	N/A	ANDA	ANDA079137	Zydus Lifesciences Limited	VALACYCLOVIR HYDROCHLORIDE	1000 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65841-630-10)
65841-630-34	65841-630	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20180405	N/A	ANDA	ANDA079137	Zydus Lifesciences Limited	VALACYCLOVIR HYDROCHLORIDE	1000 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (65841-630-34)