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=ANDA211890"
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
63629-8891-3 63629-8891 HUMAN PRESCRIPTION DRUG Ibuprofen and famotidine Ibuprofen and famotidine TABLET, FILM COATED ORAL 20230915 N/A ANDA ANDA211890 Bryant Ranch Prepack FAMOTIDINE; IBUPROFEN 26.6 mg/1; 800 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63629-8891-3)
68788-8897-9 68788-8897 HUMAN PRESCRIPTION DRUG Ibuprofen and famotidine Ibuprofen and famotidine TABLET, FILM COATED ORAL 20250801 N/A ANDA ANDA211890 Preferred Pharmaceuticals Inc. FAMOTIDINE; IBUPROFEN 26.6 mg/1; 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-8897-9)
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