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
71335-0775-1	71335-0775	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20180413	N/A	ANDA	ANDA207662	Bryant Ranch Prepack	OLMESARTAN MEDOXOMIL	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0775-1)
71335-0775-2	71335-0775	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20180808	N/A	ANDA	ANDA207662	Bryant Ranch Prepack	OLMESARTAN MEDOXOMIL	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0775-2)
71335-0775-3	71335-0775	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20200706	N/A	ANDA	ANDA207662	Bryant Ranch Prepack	OLMESARTAN MEDOXOMIL	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0775-3)
71335-0775-4	71335-0775	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20211227	N/A	ANDA	ANDA207662	Bryant Ranch Prepack	OLMESARTAN MEDOXOMIL	20 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71335-0775-4)
71335-0817-1	71335-0817	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA207662	Bryant Ranch Prepack	OLMESARTAN MEDOXOMIL	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0817-1)
71335-0817-2	71335-0817	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA207662	Bryant Ranch Prepack	OLMESARTAN MEDOXOMIL	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0817-2)
71335-0817-3	71335-0817	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA207662	Bryant Ranch Prepack	OLMESARTAN MEDOXOMIL	40 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (71335-0817-3)