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
42571-201-30	42571-201	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20200203	N/A	ANDA	ANDA206372	Micro Labs Limited	OLMESARTAN MEDOXOMIL	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (42571-201-30)
42571-201-90	42571-201	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20200203	N/A	ANDA	ANDA206372	Micro Labs Limited	OLMESARTAN MEDOXOMIL	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (42571-201-90)
42571-202-05	42571-202	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20200203	N/A	ANDA	ANDA206372	Micro Labs Limited	OLMESARTAN MEDOXOMIL	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (42571-202-05)
42571-202-10	42571-202	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20200203	N/A	ANDA	ANDA206372	Micro Labs Limited	OLMESARTAN MEDOXOMIL	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (42571-202-10)
42571-202-11	42571-202	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20200203	N/A	ANDA	ANDA206372	Micro Labs Limited	OLMESARTAN MEDOXOMIL	20 mg/1	10 BLISTER PACK in 1 CARTON (42571-202-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK (42571-202-32)
42571-202-30	42571-202	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20200203	N/A	ANDA	ANDA206372	Micro Labs Limited	OLMESARTAN MEDOXOMIL	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (42571-202-30)
42571-202-90	42571-202	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20200203	N/A	ANDA	ANDA206372	Micro Labs Limited	OLMESARTAN MEDOXOMIL	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (42571-202-90)
42571-203-05	42571-203	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20200203	N/A	ANDA	ANDA206372	Micro Labs Limited	OLMESARTAN MEDOXOMIL	40 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (42571-203-05)
42571-203-10	42571-203	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20200203	N/A	ANDA	ANDA206372	Micro Labs Limited	OLMESARTAN MEDOXOMIL	40 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (42571-203-10)
42571-203-11	42571-203	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20200203	N/A	ANDA	ANDA206372	Micro Labs Limited	OLMESARTAN MEDOXOMIL	40 mg/1	10 BLISTER PACK in 1 CARTON (42571-203-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK (42571-203-32)
42571-203-30	42571-203	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20200203	N/A	ANDA	ANDA206372	Micro Labs Limited	OLMESARTAN MEDOXOMIL	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (42571-203-30)
42571-203-90	42571-203	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20200203	N/A	ANDA	ANDA206372	Micro Labs Limited	OLMESARTAN MEDOXOMIL	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (42571-203-90)
42571-201-11	42571-201	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20200203	N/A	ANDA	ANDA206372	Micro Labs Limited	OLMESARTAN MEDOXOMIL	5 mg/1	10 BLISTER PACK in 1 CARTON (42571-201-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK (42571-201-32)
42571-201-10	42571-201	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20200203	N/A	ANDA	ANDA206372	Micro Labs Limited	OLMESARTAN MEDOXOMIL	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (42571-201-10)
42571-201-05	42571-201	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20200203	N/A	ANDA	ANDA206372	Micro Labs Limited	OLMESARTAN MEDOXOMIL	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (42571-201-05)