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=ANDA075511"
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
71205-781-60 71205-781 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20230327 N/A ANDA ANDA075511 Proficient Rx LP FAMOTIDINE 40 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-781-60)
71205-781-90 71205-781 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20230327 N/A ANDA ANDA075511 Proficient Rx LP FAMOTIDINE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-781-90)
50090-1044-0 50090-1044 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA075511 A-S Medication Solutions FAMOTIDINE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-1044-0)
50090-1044-1 50090-1044 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA075511 A-S Medication Solutions FAMOTIDINE 20 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (50090-1044-1)
50090-1044-2 50090-1044 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA075511 A-S Medication Solutions FAMOTIDINE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-1044-2)
50090-1044-3 50090-1044 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20181005 N/A ANDA ANDA075511 A-S Medication Solutions FAMOTIDINE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-1044-3)
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