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=ANDA204901"
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
82804-103-90 82804-103 HUMAN PRESCRIPTION DRUG Losartan Potassium and Hydrochlorothiazide losartan potassium and hydrochlorothiazide TABLET, FILM COATED ORAL 20240507 N/A ANDA ANDA204901 Proficient Rx LP HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (82804-103-90)
71335-2560-1 71335-2560 HUMAN PRESCRIPTION DRUG Losartan Potassium and Hydrochlorothiazide losartan potassium and hydrochlorothiazide TABLET, FILM COATED ORAL 20250124 N/A ANDA ANDA204901 Bryant Ranch Prepack HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 25 mg/1; 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-2560-1)
71335-2560-2 71335-2560 HUMAN PRESCRIPTION DRUG Losartan Potassium and Hydrochlorothiazide losartan potassium and hydrochlorothiazide TABLET, FILM COATED ORAL 20250124 N/A ANDA ANDA204901 Bryant Ranch Prepack HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 25 mg/1; 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-2560-2)
71335-2560-3 71335-2560 HUMAN PRESCRIPTION DRUG Losartan Potassium and Hydrochlorothiazide losartan potassium and hydrochlorothiazide TABLET, FILM COATED ORAL 20250124 N/A ANDA ANDA204901 Bryant Ranch Prepack HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 25 mg/1; 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-2560-3)
70518-3420-4 70518-3420 HUMAN PRESCRIPTION DRUG Losartan Potassium and Hydrochlorothiazide losartan potassium and hydrochlorothiazide TABLET, FILM COATED ORAL 20250913 N/A ANDA ANDA204901 REMEDYREPACK INC. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 25 mg/1; 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3420-4)
43547-424-03 43547-424 HUMAN PRESCRIPTION DRUG Losartan Potassium and Hydrochlorothiazide losartan potassium and hydrochlorothiazide TABLET, FILM COATED ORAL 20180215 N/A ANDA ANDA204901 Solco Healthcare US, LLC HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 25 mg/1; 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (43547-424-03)
43547-424-09 43547-424 HUMAN PRESCRIPTION DRUG Losartan Potassium and Hydrochlorothiazide losartan potassium and hydrochlorothiazide TABLET, FILM COATED ORAL 20180215 N/A ANDA ANDA204901 Solco Healthcare US, LLC HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 25 mg/1; 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (43547-424-09)
43547-424-11 43547-424 HUMAN PRESCRIPTION DRUG Losartan Potassium and Hydrochlorothiazide losartan potassium and hydrochlorothiazide TABLET, FILM COATED ORAL 20180215 N/A ANDA ANDA204901 Solco Healthcare US, LLC HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 25 mg/1; 100 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (43547-424-11)
60760-572-90 60760-572 HUMAN PRESCRIPTION DRUG Losartan Potassium and Hydrochlorothiazide losartan potassium and hydrochlorothiazide TABLET, FILM COATED ORAL 20220930 N/A ANDA ANDA204901 ST. MARY'S MEDICAL PARK PHARMACY HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 25 mg/1; 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-572-90)
83008-086-90 83008-086 HUMAN PRESCRIPTION DRUG Losartan Potassium and Hydrochlorothiazide losartan potassium and hydrochlorothiazide TABLET, FILM COATED ORAL 20240828 20270321 ANDA ANDA204901 Quality Care Products, LLC HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 25 mg/1; 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (83008-086-90)
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