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
65862-737-03	65862-737	HUMAN PRESCRIPTION DRUG	Amlodipine and valsartan	Amlodipine and valsartan	TABLET, FILM COATED	ORAL	20160422	N/A	ANDA	ANDA206512	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; VALSARTAN	5 mg/1; 160 mg/1	3 BLISTER PACK in 1 CARTON (65862-737-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-737-10)
65862-737-30	65862-737	HUMAN PRESCRIPTION DRUG	Amlodipine and valsartan	Amlodipine and valsartan	TABLET, FILM COATED	ORAL	20160422	N/A	ANDA	ANDA206512	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; VALSARTAN	5 mg/1; 160 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-737-30)
65862-737-90	65862-737	HUMAN PRESCRIPTION DRUG	Amlodipine and valsartan	Amlodipine and valsartan	TABLET, FILM COATED	ORAL	20160422	N/A	ANDA	ANDA206512	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; VALSARTAN	5 mg/1; 160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-737-90)
65862-738-03	65862-738	HUMAN PRESCRIPTION DRUG	Amlodipine and valsartan	Amlodipine and valsartan	TABLET, FILM COATED	ORAL	20160422	N/A	ANDA	ANDA206512	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; VALSARTAN	5 mg/1; 320 mg/1	3 BLISTER PACK in 1 CARTON (65862-738-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-738-10)
65862-738-30	65862-738	HUMAN PRESCRIPTION DRUG	Amlodipine and valsartan	Amlodipine and valsartan	TABLET, FILM COATED	ORAL	20160422	N/A	ANDA	ANDA206512	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; VALSARTAN	5 mg/1; 320 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-738-30)
65862-738-90	65862-738	HUMAN PRESCRIPTION DRUG	Amlodipine and valsartan	Amlodipine and valsartan	TABLET, FILM COATED	ORAL	20160422	N/A	ANDA	ANDA206512	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; VALSARTAN	5 mg/1; 320 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-738-90)
65862-739-03	65862-739	HUMAN PRESCRIPTION DRUG	Amlodipine and valsartan	Amlodipine and valsartan	TABLET, FILM COATED	ORAL	20160422	N/A	ANDA	ANDA206512	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; VALSARTAN	10 mg/1; 160 mg/1	3 BLISTER PACK in 1 CARTON (65862-739-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-739-10)
65862-739-30	65862-739	HUMAN PRESCRIPTION DRUG	Amlodipine and valsartan	Amlodipine and valsartan	TABLET, FILM COATED	ORAL	20160422	N/A	ANDA	ANDA206512	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; VALSARTAN	10 mg/1; 160 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-739-30)
65862-739-90	65862-739	HUMAN PRESCRIPTION DRUG	Amlodipine and valsartan	Amlodipine and valsartan	TABLET, FILM COATED	ORAL	20160422	N/A	ANDA	ANDA206512	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; VALSARTAN	10 mg/1; 160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-739-90)
65862-740-03	65862-740	HUMAN PRESCRIPTION DRUG	Amlodipine and valsartan	Amlodipine and valsartan	TABLET, FILM COATED	ORAL	20160422	N/A	ANDA	ANDA206512	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; VALSARTAN	10 mg/1; 320 mg/1	3 BLISTER PACK in 1 CARTON (65862-740-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-740-10)
65862-740-30	65862-740	HUMAN PRESCRIPTION DRUG	Amlodipine and valsartan	Amlodipine and valsartan	TABLET, FILM COATED	ORAL	20160422	N/A	ANDA	ANDA206512	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; VALSARTAN	10 mg/1; 320 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-740-30)
65862-740-90	65862-740	HUMAN PRESCRIPTION DRUG	Amlodipine and valsartan	Amlodipine and valsartan	TABLET, FILM COATED	ORAL	20160422	N/A	ANDA	ANDA206512	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; VALSARTAN	10 mg/1; 320 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-740-90)