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
62332-214-91	62332-214	HUMAN PRESCRIPTION DRUG	Amlodipine besylate and Olmesartran medoxomil	Amlodipine besylate and Olmesartran medoxomil	TABLET, FILM COATED	ORAL	20170718	N/A	ANDA	ANDA207073	Alembic Pharmaceuticals Inc.	AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL	10 mg/1; 20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (62332-214-91)
46708-215-30	46708-215	HUMAN PRESCRIPTION DRUG	Amlodipine besylate and Olmesartran medoxomil	Amlodipine besylate and Olmesartran medoxomil	TABLET, FILM COATED	ORAL	20170718	N/A	ANDA	ANDA207073	Alembic Pharmaceuticals Limited	AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL	10 mg/1; 40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (46708-215-30)
46708-215-90	46708-215	HUMAN PRESCRIPTION DRUG	Amlodipine besylate and Olmesartran medoxomil	Amlodipine besylate and Olmesartran medoxomil	TABLET, FILM COATED	ORAL	20170718	N/A	ANDA	ANDA207073	Alembic Pharmaceuticals Limited	AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL	10 mg/1; 40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (46708-215-90)
46708-215-91	46708-215	HUMAN PRESCRIPTION DRUG	Amlodipine besylate and Olmesartran medoxomil	Amlodipine besylate and Olmesartran medoxomil	TABLET, FILM COATED	ORAL	20170718	N/A	ANDA	ANDA207073	Alembic Pharmaceuticals Limited	AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL	10 mg/1; 40 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (46708-215-91)