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
65862-857-30	65862-857	HUMAN PRESCRIPTION DRUG	Amlodipine and Olmesartan Medoxomil	Amlodipine and Olmesartan Medoxomil	TABLET, FILM COATED	ORAL	20170515	N/A	ANDA	ANDA206906	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL	10 mg/1; 40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-857-30)
65862-854-30	65862-854	HUMAN PRESCRIPTION DRUG	Amlodipine and Olmesartan Medoxomil	Amlodipine and Olmesartan Medoxomil	TABLET, FILM COATED	ORAL	20170515	N/A	ANDA	ANDA206906	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL	5 mg/1; 20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-854-30)
65862-856-30	65862-856	HUMAN PRESCRIPTION DRUG	Amlodipine and Olmesartan Medoxomil	Amlodipine and Olmesartan Medoxomil	TABLET, FILM COATED	ORAL	20170515	N/A	ANDA	ANDA206906	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL	10 mg/1; 20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-856-30)
65862-855-30	65862-855	HUMAN PRESCRIPTION DRUG	Amlodipine and Olmesartan Medoxomil	Amlodipine and Olmesartan Medoxomil	TABLET, FILM COATED	ORAL	20170515	N/A	ANDA	ANDA206906	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL	5 mg/1; 40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-855-30)