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
31722-854-30	31722-854	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL	OLMESARTAN MEDOXOMIL	TABLET, FILM COATED	ORAL	20250523	N/A	ANDA	ANDA205499	Camber Pharmaceuticals, Inc.	OLMESARTAN MEDOXOMIL	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (31722-854-30)
31722-854-90	31722-854	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL	OLMESARTAN MEDOXOMIL	TABLET, FILM COATED	ORAL	20250523	N/A	ANDA	ANDA205499	Camber Pharmaceuticals, Inc.	OLMESARTAN MEDOXOMIL	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (31722-854-90)
31722-853-30	31722-853	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL	OLMESARTAN MEDOXOMIL	TABLET, FILM COATED	ORAL	20250523	N/A	ANDA	ANDA205499	Camber Pharmaceuticals, Inc.	OLMESARTAN MEDOXOMIL	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (31722-853-30)
31722-853-90	31722-853	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL	OLMESARTAN MEDOXOMIL	TABLET, FILM COATED	ORAL	20250523	N/A	ANDA	ANDA205499	Camber Pharmaceuticals, Inc.	OLMESARTAN MEDOXOMIL	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (31722-853-90)
31722-852-30	31722-852	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL	OLMESARTAN MEDOXOMIL	TABLET, FILM COATED	ORAL	20250523	N/A	ANDA	ANDA205499	Camber Pharmaceuticals, Inc.	OLMESARTAN MEDOXOMIL	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (31722-852-30)
31722-852-90	31722-852	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL	OLMESARTAN MEDOXOMIL	TABLET, FILM COATED	ORAL	20250523	N/A	ANDA	ANDA205499	Camber Pharmaceuticals, Inc.	OLMESARTAN MEDOXOMIL	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (31722-852-90)