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
27808-277-01	27808-277	HUMAN PRESCRIPTION DRUG	Olmesartan Medoxomil	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20230520	20250131	ANDA	ANDA210552	Tris Pharma, Inc.	OLMESARTAN MEDOXOMIL	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (27808-277-01)
27808-277-02	27808-277	HUMAN PRESCRIPTION DRUG	Olmesartan Medoxomil	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20230520	20250131	ANDA	ANDA210552	Tris Pharma, Inc.	OLMESARTAN MEDOXOMIL	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (27808-277-02)
27808-276-01	27808-276	HUMAN PRESCRIPTION DRUG	Olmesartan Medoxomil	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20230520	20250131	ANDA	ANDA210552	Tris Pharma, Inc.	OLMESARTAN MEDOXOMIL	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (27808-276-01)
27808-276-02	27808-276	HUMAN PRESCRIPTION DRUG	Olmesartan Medoxomil	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20230520	20250131	ANDA	ANDA210552	Tris Pharma, Inc.	OLMESARTAN MEDOXOMIL	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (27808-276-02)
27808-275-01	27808-275	HUMAN PRESCRIPTION DRUG	Olmesartan Medoxomil	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20230520	20250131	ANDA	ANDA210552	Tris Pharma, Inc.	OLMESARTAN MEDOXOMIL	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (27808-275-01)
27808-275-02	27808-275	HUMAN PRESCRIPTION DRUG	Olmesartan Medoxomil	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20230520	20250131	ANDA	ANDA210552	Tris Pharma, Inc.	OLMESARTAN MEDOXOMIL	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (27808-275-02)