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
43063-771-20	43063-771	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20180326	N/A	ANDA	ANDA203047	PD-Rx Pharmaceuticals, Inc.	VALACYCLOVIR HYDROCHLORIDE	1 g/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-771-20)
43063-771-21	43063-771	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20170811	N/A	ANDA	ANDA203047	PD-Rx Pharmaceuticals, Inc.	VALACYCLOVIR HYDROCHLORIDE	1 g/1	21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-771-21)
68071-4805-1	68071-4805	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20190318	N/A	ANDA	ANDA203047	NuCare Pharmaceuticals,Inc.	VALACYCLOVIR HYDROCHLORIDE	1 g/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-4805-1)
68071-4805-6	68071-4805	HUMAN PRESCRIPTION DRUG	Valacyclovir	Valacyclovir	TABLET, FILM COATED	ORAL	20190318	N/A	ANDA	ANDA203047	NuCare Pharmaceuticals,Inc.	VALACYCLOVIR HYDROCHLORIDE	1 g/1	60 TABLET, FILM COATED in 1 BOTTLE (68071-4805-6)
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)
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)
31722-704-05	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)