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=ANDA213483"
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
72205-337-18 72205-337 HUMAN PRESCRIPTION DRUG Ivabradine Ivabradine TABLET, FILM COATED ORAL 20250701 N/A ANDA ANDA213483 Novadoz Pharmaceuticals LLC IVABRADINE HYDROCHLORIDE 7.5 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (72205-337-18)
72205-337-60 72205-337 HUMAN PRESCRIPTION DRUG Ivabradine Ivabradine TABLET, FILM COATED ORAL 20250701 N/A ANDA ANDA213483 Novadoz Pharmaceuticals LLC IVABRADINE HYDROCHLORIDE 7.5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (72205-337-60)
72205-336-18 72205-336 HUMAN PRESCRIPTION DRUG Ivabradine Ivabradine TABLET, FILM COATED ORAL 20250701 N/A ANDA ANDA213483 Novadoz Pharmaceuticals LLC IVABRADINE HYDROCHLORIDE 5 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (72205-336-18)
72205-336-60 72205-336 HUMAN PRESCRIPTION DRUG Ivabradine Ivabradine TABLET, FILM COATED ORAL 20250701 N/A ANDA ANDA213483 Novadoz Pharmaceuticals LLC IVABRADINE HYDROCHLORIDE 5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (72205-336-60)
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