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=ANDA212434"
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
50090-5812-0 50090-5812 HUMAN PRESCRIPTION DRUG Anastrozole Anastrozole TABLET, FILM COATED ORAL 20211018 N/A ANDA ANDA212434 A-S Medication Solutions ANASTROZOLE 1 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-5812-0)
50090-5812-1 50090-5812 HUMAN PRESCRIPTION DRUG Anastrozole Anastrozole TABLET, FILM COATED ORAL 20211018 N/A ANDA ANDA212434 A-S Medication Solutions ANASTROZOLE 1 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-5812-1)
59651-236-30 59651-236 HUMAN PRESCRIPTION DRUG Anastrozole Anastrozole TABLET, FILM COATED ORAL 20200724 N/A ANDA ANDA212434 Aurobindo Pharma Limited ANASTROZOLE 1 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (59651-236-30)
59651-236-90 59651-236 HUMAN PRESCRIPTION DRUG Anastrozole Anastrozole TABLET, FILM COATED ORAL 20200724 N/A ANDA ANDA212434 Aurobindo Pharma Limited ANASTROZOLE 1 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (59651-236-90)
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