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=ANDA207206"
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
51655-597-26 51655-597 HUMAN PRESCRIPTION DRUG Metoprolol Succinate Metoprolol Succinate TABLET, EXTENDED RELEASE ORAL 20220330 N/A ANDA ANDA207206 Northwind Pharmaceuticals, LLC METOPROLOL TARTRATE 50 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-597-26)
51655-597-52 51655-597 HUMAN PRESCRIPTION DRUG Metoprolol Succinate Metoprolol Succinate TABLET, EXTENDED RELEASE ORAL 20210203 N/A ANDA ANDA207206 Northwind Pharmaceuticals, LLC METOPROLOL TARTRATE 50 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-597-52)
51655-615-26 51655-615 HUMAN PRESCRIPTION DRUG Metoprolol Succinate Metoprolol Succinate TABLET, EXTENDED RELEASE ORAL 20210226 N/A ANDA ANDA207206 Northwind Pharmaceuticals, LLC METOPROLOL TARTRATE 100 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-615-26)
51655-615-52 51655-615 HUMAN PRESCRIPTION DRUG Metoprolol Succinate Metoprolol Succinate TABLET, EXTENDED RELEASE ORAL 20210219 N/A ANDA ANDA207206 Northwind Pharmaceuticals, LLC METOPROLOL TARTRATE 100 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-615-52)
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