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
68788-8187-3 68788-8187 HUMAN PRESCRIPTION DRUG Losartan Potassium and Hydrochlorothiazide losartan potassium and hydrochlorothiazide TABLET, FILM COATED ORAL 20220510 N/A ANDA ANDA204901 Preferred Pharmaceuticals Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-8187-3)
68788-8187-6 68788-8187 HUMAN PRESCRIPTION DRUG Losartan Potassium and Hydrochlorothiazide losartan potassium and hydrochlorothiazide TABLET, FILM COATED ORAL 20220510 N/A ANDA ANDA204901 Preferred Pharmaceuticals Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-8187-6)
68788-8187-9 68788-8187 HUMAN PRESCRIPTION DRUG Losartan Potassium and Hydrochlorothiazide losartan potassium and hydrochlorothiazide TABLET, FILM COATED ORAL 20220510 N/A ANDA ANDA204901 Preferred Pharmaceuticals Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-8187-9)
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)
43547-425-03 43547-425 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 12.5 mg/1; 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (43547-425-03)
43547-425-09 43547-425 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 12.5 mg/1; 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (43547-425-09)
43547-425-11 43547-425 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 12.5 mg/1; 100 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (43547-425-11)
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