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=ANDA214051"
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
51407-592-60 51407-592 HUMAN PRESCRIPTION DRUG IVABRADINE IVABRADINE TABLET, FILM COATED ORAL 20240829 N/A ANDA ANDA214051 Golden State Medical Supply, Inc. IVABRADINE HYDROCHLORIDE 5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (51407-592-60)
51407-593-60 51407-593 HUMAN PRESCRIPTION DRUG IVABRADINE IVABRADINE TABLET, FILM COATED ORAL 20240829 N/A ANDA ANDA214051 Golden State Medical Supply, Inc. IVABRADINE HYDROCHLORIDE 7.5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (51407-593-60)
50742-363-60 50742-363 HUMAN PRESCRIPTION DRUG IVABRADINE IVABRADINE TABLET, FILM COATED ORAL 20240715 N/A ANDA ANDA214051 Ingenus Pharmaceuticals, LLC IVABRADINE HYDROCHLORIDE 7.5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50742-363-60)
50742-362-60 50742-362 HUMAN PRESCRIPTION DRUG IVABRADINE IVABRADINE TABLET, FILM COATED ORAL 20240715 N/A ANDA ANDA214051 Ingenus Pharmaceuticals, LLC IVABRADINE HYDROCHLORIDE 5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50742-362-60)
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