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=NDA205879"
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
50458-941-01 50458-941 HUMAN PRESCRIPTION DRUG INVOKAMET XR canagliflozin and metformin hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160920 N/A NDA NDA205879 Janssen Pharmaceuticals, Inc. CANAGLIFLOZIN; METFORMIN HYDROCHLORIDE 50 mg/1; 1000 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50458-941-01)
50458-942-01 50458-942 HUMAN PRESCRIPTION DRUG INVOKAMET XR canagliflozin and metformin hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160920 N/A NDA NDA205879 Janssen Pharmaceuticals, Inc. CANAGLIFLOZIN; METFORMIN HYDROCHLORIDE 150 mg/1; 500 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50458-942-01)
50458-943-01 50458-943 HUMAN PRESCRIPTION DRUG INVOKAMET XR canagliflozin and metformin hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160920 N/A NDA NDA205879 Janssen Pharmaceuticals, Inc. CANAGLIFLOZIN; METFORMIN HYDROCHLORIDE 150 mg/1; 1000 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50458-943-01)
50458-940-01 50458-940 HUMAN PRESCRIPTION DRUG INVOKAMET XR canagliflozin and metformin hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160920 N/A NDA NDA205879 Janssen Pharmaceuticals, Inc. CANAGLIFLOZIN; METFORMIN HYDROCHLORIDE 50 mg/1; 500 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50458-940-01)
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