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
0078-0489-15	0078-0489	HUMAN PRESCRIPTION DRUG	Exforge	amlodipine besylate and valsartan	TABLET, FILM COATED	ORAL	20070620	N/A	NDA	NDA021990	Novartis Pharmaceuticals Corporation	AMLODIPINE BESYLATE; VALSARTAN	10 mg/1; 160 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0078-0489-15)
0078-0490-15	0078-0490	HUMAN PRESCRIPTION DRUG	Exforge	amlodipine besylate and valsartan	TABLET, FILM COATED	ORAL	20070620	N/A	NDA	NDA021990	Novartis Pharmaceuticals Corporation	AMLODIPINE BESYLATE; VALSARTAN	5 mg/1; 320 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0078-0490-15)
0078-0488-15	0078-0488	HUMAN PRESCRIPTION DRUG	Exforge	amlodipine besylate and valsartan	TABLET, FILM COATED	ORAL	20070620	N/A	NDA	NDA021990	Novartis Pharmaceuticals Corporation	AMLODIPINE BESYLATE; VALSARTAN	5 mg/1; 160 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0078-0488-15)
0078-0491-15	0078-0491	HUMAN PRESCRIPTION DRUG	Exforge	amlodipine besylate and valsartan	TABLET, FILM COATED	ORAL	20070620	N/A	NDA	NDA021990	Novartis Pharmaceuticals Corporation	AMLODIPINE BESYLATE; VALSARTAN	10 mg/1; 320 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0078-0491-15)