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）
检索条件:" 注册申请号=ANDA205391"
符合检索条件的记录共 20 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
65862-779-78 65862-779 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil and Hydrochlorothiazide Olmesartan Medoxomil and Hydrochlorothiazide TABLET, FILM COATED ORAL 20170424 N/A ANDA ANDA205391 Aurobindo Pharma Limited HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 20 mg/1 10 BLISTER PACK in 1 CARTON (65862-779-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-779-10)
65862-779-90 65862-779 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil and Hydrochlorothiazide Olmesartan Medoxomil and Hydrochlorothiazide TABLET, FILM COATED ORAL 20170424 N/A ANDA ANDA205391 Aurobindo Pharma Limited HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65862-779-90)
65862-779-99 65862-779 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil and Hydrochlorothiazide Olmesartan Medoxomil and Hydrochlorothiazide TABLET, FILM COATED ORAL 20170424 N/A ANDA ANDA205391 Aurobindo Pharma Limited HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65862-779-99)
65862-780-30 65862-780 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil and Hydrochlorothiazide Olmesartan Medoxomil and Hydrochlorothiazide TABLET, FILM COATED ORAL 20170424 N/A ANDA ANDA205391 Aurobindo Pharma Limited HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-780-30)
65862-780-78 65862-780 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil and Hydrochlorothiazide Olmesartan Medoxomil and Hydrochlorothiazide TABLET, FILM COATED ORAL 20170424 N/A ANDA ANDA205391 Aurobindo Pharma Limited HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 40 mg/1 10 BLISTER PACK in 1 CARTON (65862-780-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-780-10)
65862-780-90 65862-780 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil and Hydrochlorothiazide Olmesartan Medoxomil and Hydrochlorothiazide TABLET, FILM COATED ORAL 20170424 N/A ANDA ANDA205391 Aurobindo Pharma Limited HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65862-780-90)
65862-780-99 65862-780 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil and Hydrochlorothiazide Olmesartan Medoxomil and Hydrochlorothiazide TABLET, FILM COATED ORAL 20170424 N/A ANDA ANDA205391 Aurobindo Pharma Limited HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 40 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65862-780-99)
65862-781-30 65862-781 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil and Hydrochlorothiazide Olmesartan Medoxomil and Hydrochlorothiazide TABLET, FILM COATED ORAL 20170424 N/A ANDA ANDA205391 Aurobindo Pharma Limited HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 25 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-781-30)
65862-781-78 65862-781 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil and Hydrochlorothiazide Olmesartan Medoxomil and Hydrochlorothiazide TABLET, FILM COATED ORAL 20170424 N/A ANDA ANDA205391 Aurobindo Pharma Limited HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 25 mg/1; 40 mg/1 10 BLISTER PACK in 1 CARTON (65862-781-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-781-10)
65862-781-90 65862-781 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil and Hydrochlorothiazide Olmesartan Medoxomil and Hydrochlorothiazide TABLET, FILM COATED ORAL 20170424 N/A ANDA ANDA205391 Aurobindo Pharma Limited HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 25 mg/1; 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65862-781-90)
65862-781-99 65862-781 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil and Hydrochlorothiazide Olmesartan Medoxomil and Hydrochlorothiazide TABLET, FILM COATED ORAL 20170424 N/A ANDA ANDA205391 Aurobindo Pharma Limited HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 25 mg/1; 40 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65862-781-99)
50090-3701-0 50090-3701 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil and Hydrochlorothiazide Olmesartan Medoxomil and Hydrochlorothiazide TABLET, FILM COATED ORAL 20191009 N/A ANDA ANDA205391 A-S Medication Solutions HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-3701-0)
50090-3561-0 50090-3561 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil and Hydrochlorothiazide Olmesartan Medoxomil and Hydrochlorothiazide TABLET, FILM COATED ORAL 20180830 N/A ANDA ANDA205391 A-S Medication Solutions HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-3561-0)
65862-779-30 65862-779 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil and Hydrochlorothiazide Olmesartan Medoxomil and Hydrochlorothiazide TABLET, FILM COATED ORAL 20170424 N/A ANDA ANDA205391 Aurobindo Pharma Limited HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-779-30)
50090-3701-1 50090-3701 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil and Hydrochlorothiazide Olmesartan Medoxomil and Hydrochlorothiazide TABLET, FILM COATED ORAL 20181022 N/A ANDA ANDA205391 A-S Medication Solutions HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-3701-1)
50090-4377-0 50090-4377 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil and Hydrochlorothiazide Olmesartan Medoxomil and Hydrochlorothiazide TABLET, FILM COATED ORAL 20190621 N/A ANDA ANDA205391 A-S Medication Solutions HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 25 mg/1; 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-4377-0)
71335-0845-3 71335-0845 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil and Hydrochlorothiazide Olmesartan Medoxomil and Hydrochlorothiazide TABLET, FILM COATED ORAL 20240529 N/A ANDA ANDA205391 Bryant Ranch Prepack HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 40 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (71335-0845-3)
71335-0845-1 71335-0845 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil and Hydrochlorothiazide Olmesartan Medoxomil and Hydrochlorothiazide TABLET, FILM COATED ORAL 20240529 N/A ANDA ANDA205391 Bryant Ranch Prepack HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0845-1)
71335-0845-2 71335-0845 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil and Hydrochlorothiazide Olmesartan Medoxomil and Hydrochlorothiazide TABLET, FILM COATED ORAL 20180531 N/A ANDA ANDA205391 Bryant Ranch Prepack HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-0845-2)
70518-3889-0 70518-3889 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil and Hydrochlorothiazide Olmesartan Medoxomil and Hydrochlorothiazide TABLET, FILM COATED ORAL 20231009 N/A ANDA ANDA205391 REMEDYREPACK INC. HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 12.5 mg/1; 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3889-0)
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