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
50090-3487-1	50090-3487	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20180618	N/A	ANDA	ANDA207662	A-S Medication Solutions	OLMESARTAN MEDOXOMIL	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3487-1)
72189-137-30	72189-137	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL	OLMESARTAN MEDOXOMIL	TABLET, FILM COATED	ORAL	20201202	N/A	ANDA	ANDA207662	direct rx	OLMESARTAN MEDOXOMIL	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72189-137-30)
72189-137-90	72189-137	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL	OLMESARTAN MEDOXOMIL	TABLET, FILM COATED	ORAL	20201202	N/A	ANDA	ANDA207662	direct rx	OLMESARTAN MEDOXOMIL	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72189-137-90)
16729-322-10	16729-322	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20170427	N/A	ANDA	ANDA207662	Accord Healthcare Inc.	OLMESARTAN MEDOXOMIL	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16729-322-10)
16729-322-15	16729-322	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20170427	N/A	ANDA	ANDA207662	Accord Healthcare Inc.	OLMESARTAN MEDOXOMIL	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16729-322-15)
16729-322-17	16729-322	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20170427	N/A	ANDA	ANDA207662	Accord Healthcare Inc.	OLMESARTAN MEDOXOMIL	40 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16729-322-17)