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
0078-0559-15	0078-0559	HUMAN PRESCRIPTION DRUG	Exforge HCT	amlodipine valsartan and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20090404	N/A	NDA	NDA022314	Novartis Pharmaceuticals Corporation	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN	5 mg/1; 12.5 mg/1; 160 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0078-0559-15)
0078-0560-15	0078-0560	HUMAN PRESCRIPTION DRUG	Exforge HCT	amlodipine valsartan and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20090404	N/A	NDA	NDA022314	Novartis Pharmaceuticals Corporation	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN	5 mg/1; 25 mg/1; 160 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0078-0560-15)
0078-0561-15	0078-0561	HUMAN PRESCRIPTION DRUG	Exforge HCT	amlodipine valsartan and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20090404	N/A	NDA	NDA022314	Novartis Pharmaceuticals Corporation	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN	10 mg/1; 12.5 mg/1; 160 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0078-0561-15)
0078-0562-15	0078-0562	HUMAN PRESCRIPTION DRUG	Exforge HCT	amlodipine valsartan and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20090404	N/A	NDA	NDA022314	Novartis Pharmaceuticals Corporation	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN	10 mg/1; 25 mg/1; 160 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0078-0562-15)
0078-0563-15	0078-0563	HUMAN PRESCRIPTION DRUG	Exforge HCT	amlodipine valsartan and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20090404	N/A	NDA	NDA022314	Novartis Pharmaceuticals Corporation	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN	10 mg/1; 25 mg/1; 320 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0078-0563-15)