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=ANDA076704"
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
51407-109-10 51407-109 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate metoprolol tartrate TABLET, FILM COATED ORAL 20210310 N/A ANDA ANDA076704 Golden State Medical Supply, Inc. METOPROLOL TARTRATE 25 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51407-109-10)
71610-559-53 71610-559 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate metoprolol tartrate TABLET, FILM COATED ORAL 20210520 N/A ANDA ANDA076704 Aphena Pharma Solutions - Tennessee, LLC METOPROLOL TARTRATE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-559-53)
71610-559-60 71610-559 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate metoprolol tartrate TABLET, FILM COATED ORAL 20210520 N/A ANDA ANDA076704 Aphena Pharma Solutions - Tennessee, LLC METOPROLOL TARTRATE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-559-60)
71610-559-80 71610-559 HUMAN PRESCRIPTION DRUG Metoprolol Tartrate metoprolol tartrate TABLET, FILM COATED ORAL 20210520 N/A ANDA ANDA076704 Aphena Pharma Solutions - Tennessee, LLC METOPROLOL TARTRATE 100 mg/1 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-559-80)
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