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=NDA203214"
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
63539-016-02 63539-016 HUMAN PRESCRIPTION DRUG XELJANZ tofacitinib TABLET, FILM COATED ORAL 20180702 N/A NDA NDA203214 U.S. Pharmaceuticals TOFACITINIB CITRATE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63539-016-02)
63539-012-02 63539-012 HUMAN PRESCRIPTION DRUG XELJANZ tofacitinib TABLET, FILM COATED ORAL 20121108 N/A NDA NDA203214 U.S. Pharmaceuticals TOFACITINIB CITRATE 5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63539-012-02)
0069-1002-01 0069-1002 HUMAN PRESCRIPTION DRUG XELJANZ tofacitinib TABLET, FILM COATED ORAL 20180702 N/A NDA NDA203214 Pfizer Laboratories Div Pfizer Inc TOFACITINIB CITRATE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (0069-1002-01)
0069-1001-01 0069-1001 HUMAN PRESCRIPTION DRUG XELJANZ tofacitinib TABLET, FILM COATED ORAL 20121109 N/A NDA NDA203214 Pfizer Laboratories Div Pfizer Inc TOFACITINIB CITRATE 5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (0069-1001-01)
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