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=ANDA219332"
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
31722-496-18 31722-496 HUMAN PRESCRIPTION DRUG RIVAROXABAN RIVAROXABAN TABLET, FILM COATED ORAL 20250520 N/A ANDA ANDA219332 Camber Pharmaceuticals, Inc. RIVAROXABAN 2.5 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (31722-496-18)
31722-496-60 31722-496 HUMAN PRESCRIPTION DRUG RIVAROXABAN RIVAROXABAN TABLET, FILM COATED ORAL 20250520 N/A ANDA ANDA219332 Camber Pharmaceuticals, Inc. RIVAROXABAN 2.5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (31722-496-60)
72865-321-18 72865-321 HUMAN PRESCRIPTION DRUG RIVAROXABAN RIVAROXABAN TABLET, FILM COATED ORAL 20251217 N/A ANDA ANDA219332 XLCare Pharmaceuticals, Inc. RIVAROXABAN 2.5 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (72865-321-18)
72865-321-60 72865-321 HUMAN PRESCRIPTION DRUG RIVAROXABAN RIVAROXABAN TABLET, FILM COATED ORAL 20251217 N/A ANDA ANDA219332 XLCare Pharmaceuticals, Inc. RIVAROXABAN 2.5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (72865-321-60)
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