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=ANDA208546"
符合检索条件的记录共 4 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
72205-416-05 72205-416 HUMAN PRESCRIPTION DRUG Rivaroxaban Rivaroxaban TABLET, FILM COATED ORAL 20260318 N/A ANDA ANDA208546 Novadoz Pharmaceuticals LLC RIVAROXABAN 2.5 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (72205-416-05)
72205-416-04 72205-416 HUMAN PRESCRIPTION DRUG Rivaroxaban Rivaroxaban TABLET, FILM COATED ORAL 20260318 N/A ANDA ANDA208546 Novadoz Pharmaceuticals LLC RIVAROXABAN 2.5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (72205-416-04)
72205-416-03 72205-416 HUMAN PRESCRIPTION DRUG Rivaroxaban Rivaroxaban TABLET, FILM COATED ORAL 20260318 N/A ANDA ANDA208546 Novadoz Pharmaceuticals LLC RIVAROXABAN 2.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72205-416-03)
72205-416-02 72205-416 HUMAN PRESCRIPTION DRUG Rivaroxaban Rivaroxaban TABLET, FILM COATED ORAL 20260318 N/A ANDA ANDA208546 Novadoz Pharmaceuticals LLC RIVAROXABAN 2.5 mg/1 10 BLISTER PACK in 1 CARTON (72205-416-02) / 10 TABLET, FILM COATED in 1 BLISTER PACK
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