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=ANDA075805"
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
63629-2782-7 63629-2782 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20240905 N/A ANDA ANDA075805 Bryant Ranch Prepack FAMOTIDINE 40 mg/1 20 TABLET in 1 BOTTLE (63629-2782-7)
63629-2782-1 63629-2782 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20050314 N/A ANDA ANDA075805 Bryant Ranch Prepack FAMOTIDINE 40 mg/1 30 TABLET in 1 BOTTLE (63629-2782-1)
63629-2782-2 63629-2782 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20070626 N/A ANDA ANDA075805 Bryant Ranch Prepack FAMOTIDINE 40 mg/1 60 TABLET in 1 BOTTLE (63629-2782-2)
63629-2782-3 63629-2782 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20070716 N/A ANDA ANDA075805 Bryant Ranch Prepack FAMOTIDINE 40 mg/1 100 TABLET in 1 BOTTLE (63629-2782-3)
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