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
72162-2315-3 72162-2315 HUMAN PRESCRIPTION DRUG Losartan Potassium and Hydrochlorothiazide losartan potassium and hydrochlorothiazide TABLET, FILM COATED ORAL 20240516 N/A ANDA ANDA204901 Bryant Ranch Prepack HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72162-2315-3)
72162-2315-9 72162-2315 HUMAN PRESCRIPTION DRUG Losartan Potassium and Hydrochlorothiazide losartan potassium and hydrochlorothiazide TABLET, FILM COATED ORAL 20240516 N/A ANDA ANDA204901 Bryant Ranch Prepack HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (72162-2315-9)
42708-193-30 42708-193 HUMAN PRESCRIPTION DRUG Losartan Potassium and Hydrochlorothiazide losartan potassium and hydrochlorothiazide TABLET, FILM COATED ORAL 20260201 N/A ANDA ANDA204901 QPharma, Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-193-30)
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)
72189-325-30 72189-325 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20220216 N/A ANDA ANDA204901 Direct Rx HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72189-325-30)
72189-325-90 72189-325 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20220216 N/A ANDA ANDA204901 Direct Rx HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (72189-325-90)
72189-326-30 72189-326 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE losartan potassium and hydrochlorothiazide TABLET, FILM COATED ORAL 20220221 N/A ANDA ANDA204901 Direct Rx HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 25 mg/1; 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72189-326-30)
72189-326-90 72189-326 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE losartan potassium and hydrochlorothiazide TABLET, FILM COATED ORAL 20220221 N/A ANDA ANDA204901 Direct Rx HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 25 mg/1; 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (72189-326-90)
72189-327-90 72189-327 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20220217 N/A ANDA ANDA204901 Direct Rx HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (72189-327-90)
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