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
0713-0940-30	0713-0940	HUMAN PRESCRIPTION DRUG	Benicar	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20251001	N/A	NDA	NDA021286	Cosette Pharmaceuticals, Inc.	OLMESARTAN MEDOXOMIL	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0713-0940-30)
0713-0862-30	0713-0862	HUMAN PRESCRIPTION DRUG	Benicar	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20220901	N/A	NDA	NDA021286	Cosette Pharmaceuticals, Inc.	OLMESARTAN MEDOXOMIL	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0713-0862-30)
0713-0942-30	0713-0942	HUMAN PRESCRIPTION DRUG	Benicar	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20251201	N/A	NDA	NDA021286	Cosette Pharmaceuticals, Inc.	OLMESARTAN MEDOXOMIL	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0713-0942-30)
0713-0861-30	0713-0861	HUMAN PRESCRIPTION DRUG	Benicar	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20220901	N/A	NDA	NDA021286	Cosette Pharmaceuticals, Inc.	OLMESARTAN MEDOXOMIL	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0713-0861-30)
0713-0941-30	0713-0941	HUMAN PRESCRIPTION DRUG	Benicar	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20250801	N/A	NDA	NDA021286	Cosette Pharmaceuticals, Inc.	OLMESARTAN MEDOXOMIL	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0713-0941-30)
0713-0860-30	0713-0860	HUMAN PRESCRIPTION DRUG	Benicar	olmesartan medoxomil	TABLET, FILM COATED	ORAL	20220901	N/A	NDA	NDA021286	Cosette Pharmaceuticals, Inc.	OLMESARTAN MEDOXOMIL	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0713-0860-30)