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=ANDA078385"
符合检索条件的记录共 16 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
65841-732-40 65841-732 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20100410 N/A ANDA ANDA078385 Zydus Lifesciences Limited HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 50 mg/1 5000 TABLET, FILM COATED in 1 BOTTLE (65841-732-40)
65841-733-06 65841-733 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20100410 N/A ANDA ANDA078385 Zydus Lifesciences Limited HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 25 mg/1; 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65841-733-06)
65841-733-10 65841-733 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20100410 N/A ANDA ANDA078385 Zydus Lifesciences Limited HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 25 mg/1; 100 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65841-733-10)
65841-733-16 65841-733 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20100410 N/A ANDA ANDA078385 Zydus Lifesciences Limited HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 25 mg/1; 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65841-733-16)
65841-733-23 65841-733 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20100410 N/A ANDA ANDA078385 Zydus Lifesciences Limited HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 25 mg/1; 100 mg/1 4000 TABLET, FILM COATED in 1 BOTTLE (65841-733-23)
68382-142-06 68382-142 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20101004 N/A ANDA ANDA078385 Zydus Pharmaceuticals USA Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68382-142-06)
68382-142-10 68382-142 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20101004 N/A ANDA ANDA078385 Zydus Pharmaceuticals USA Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (68382-142-10)
68382-142-16 68382-142 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20101004 N/A ANDA ANDA078385 Zydus Pharmaceuticals USA Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68382-142-16)
68382-142-40 68382-142 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20101004 N/A ANDA ANDA078385 Zydus Pharmaceuticals USA Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 50 mg/1 5000 TABLET, FILM COATED in 1 BOTTLE (68382-142-40)
68382-143-06 68382-143 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20101004 N/A ANDA ANDA078385 Zydus Pharmaceuticals USA Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 25 mg/1; 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68382-143-06)
68382-143-10 68382-143 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20101004 N/A ANDA ANDA078385 Zydus Pharmaceuticals USA Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 25 mg/1; 100 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (68382-143-10)
68382-143-16 68382-143 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20101004 N/A ANDA ANDA078385 Zydus Pharmaceuticals USA Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 25 mg/1; 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68382-143-16)
68382-143-23 68382-143 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20101004 N/A ANDA ANDA078385 Zydus Pharmaceuticals USA Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 25 mg/1; 100 mg/1 4000 TABLET, FILM COATED in 1 BOTTLE (68382-143-23)
65841-732-16 65841-732 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20100410 N/A ANDA ANDA078385 Zydus Lifesciences Limited HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65841-732-16)
65841-732-10 65841-732 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20100410 N/A ANDA ANDA078385 Zydus Lifesciences Limited HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65841-732-10)
65841-732-06 65841-732 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20100410 N/A ANDA ANDA078385 Zydus Lifesciences Limited HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65841-732-06)
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