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=ANDA208360"
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
68382-857-05 68382-857 HUMAN PRESCRIPTION DRUG triamterene and hydrochlorothiazide triamterene and hydrochlorothiazide TABLET ORAL 20180904 N/A ANDA ANDA208360 Zydus Pharmaceuticals (USA) Inc. HYDROCHLOROTHIAZIDE; TRIAMTERENE 50 mg/1; 75 mg/1 500 TABLET in 1 BOTTLE (68382-857-05)
68382-857-10 68382-857 HUMAN PRESCRIPTION DRUG triamterene and hydrochlorothiazide triamterene and hydrochlorothiazide TABLET ORAL 20180904 N/A ANDA ANDA208360 Zydus Pharmaceuticals (USA) Inc. HYDROCHLOROTHIAZIDE; TRIAMTERENE 50 mg/1; 75 mg/1 1000 TABLET in 1 BOTTLE (68382-857-10)
68382-857-77 68382-857 HUMAN PRESCRIPTION DRUG triamterene and hydrochlorothiazide triamterene and hydrochlorothiazide TABLET ORAL 20180904 N/A ANDA ANDA208360 Zydus Pharmaceuticals (USA) Inc. HYDROCHLOROTHIAZIDE; TRIAMTERENE 50 mg/1; 75 mg/1 10 BLISTER PACK in 1 CARTON (68382-857-77) / 10 TABLET in 1 BLISTER PACK (68382-857-30)
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