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
16729-366-15	16729-366	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE	OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE	TABLET, FILM COATED	ORAL	20200921	N/A	ANDA	ANDA209281	Accord Healthcare Inc.	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (16729-366-15)
16729-367-15	16729-367	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE	OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE	TABLET, FILM COATED	ORAL	20200903	N/A	ANDA	ANDA209281	Accord Healthcare Inc.	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (16729-367-15)
16729-368-15	16729-368	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE	OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE	TABLET, FILM COATED	ORAL	20200903	N/A	ANDA	ANDA209281	Accord Healthcare Inc.	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	25 mg/1; 40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (16729-368-15)
50090-5402-0	50090-5402	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE	OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE	TABLET, FILM COATED	ORAL	20201208	N/A	ANDA	ANDA209281	A-S Medication Solutions	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-5402-0)
50090-6537-0	50090-6537	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE	OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE	TABLET, FILM COATED	ORAL	20230628	N/A	ANDA	ANDA209281	A-S Medication Solutions	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-6537-0)
50090-6537-1	50090-6537	HUMAN PRESCRIPTION DRUG	OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE	OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE	TABLET, FILM COATED	ORAL	20230628	N/A	ANDA	ANDA209281	A-S Medication Solutions	HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	12.5 mg/1; 20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-6537-1)