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=ANDA204310"
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
16714-213-01 16714-213 HUMAN PRESCRIPTION DRUG Raloxifene Hydrochloride Raloxifene Hydrochloride TABLET, FILM COATED ORAL 20150828 N/A ANDA ANDA204310 NorthStar Rx LLC RALOXIFENE HYDROCHLORIDE 60 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (16714-213-01)
16714-213-02 16714-213 HUMAN PRESCRIPTION DRUG Raloxifene Hydrochloride Raloxifene Hydrochloride TABLET, FILM COATED ORAL 20150828 N/A ANDA ANDA204310 NorthStar Rx LLC RALOXIFENE HYDROCHLORIDE 60 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16714-213-02)
16714-213-03 16714-213 HUMAN PRESCRIPTION DRUG Raloxifene Hydrochloride Raloxifene Hydrochloride TABLET, FILM COATED ORAL 20150828 N/A ANDA ANDA204310 NorthStar Rx LLC RALOXIFENE HYDROCHLORIDE 60 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (16714-213-03)
71335-2059-1 71335-2059 HUMAN PRESCRIPTION DRUG Raloxifene Hydrochloride Raloxifene Hydrochloride TABLET, FILM COATED ORAL 20220303 N/A ANDA ANDA204310 Bryant Ranch Prepack RALOXIFENE HYDROCHLORIDE 60 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-2059-1)
71335-2059-2 71335-2059 HUMAN PRESCRIPTION DRUG Raloxifene Hydrochloride Raloxifene Hydrochloride TABLET, FILM COATED ORAL 20240227 N/A ANDA ANDA204310 Bryant Ranch Prepack RALOXIFENE HYDROCHLORIDE 60 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-2059-2)
65862-709-01 65862-709 HUMAN PRESCRIPTION DRUG Raloxifene Hydrochloride Raloxifene Hydrochloride TABLET, FILM COATED ORAL 20150828 N/A ANDA ANDA204310 Aurobindo Pharma Limited RALOXIFENE HYDROCHLORIDE 60 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-709-01)
65862-709-03 65862-709 HUMAN PRESCRIPTION DRUG Raloxifene Hydrochloride Raloxifene Hydrochloride TABLET, FILM COATED ORAL 20150828 N/A ANDA ANDA204310 Aurobindo Pharma Limited RALOXIFENE HYDROCHLORIDE 60 mg/1 3 BLISTER PACK in 1 CARTON (65862-709-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-709-10)
65862-709-22 65862-709 HUMAN PRESCRIPTION DRUG Raloxifene Hydrochloride Raloxifene Hydrochloride TABLET, FILM COATED ORAL 20150828 N/A ANDA ANDA204310 Aurobindo Pharma Limited RALOXIFENE HYDROCHLORIDE 60 mg/1 2000 TABLET, FILM COATED in 1 BOTTLE (65862-709-22)
65862-709-30 65862-709 HUMAN PRESCRIPTION DRUG Raloxifene Hydrochloride Raloxifene Hydrochloride TABLET, FILM COATED ORAL 20150828 N/A ANDA ANDA204310 Aurobindo Pharma Limited RALOXIFENE HYDROCHLORIDE 60 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-709-30)
65862-709-99 65862-709 HUMAN PRESCRIPTION DRUG Raloxifene Hydrochloride Raloxifene Hydrochloride TABLET, FILM COATED ORAL 20150828 N/A ANDA ANDA204310 Aurobindo Pharma Limited RALOXIFENE HYDROCHLORIDE 60 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65862-709-99)
50090-7073-1 50090-7073 HUMAN PRESCRIPTION DRUG Raloxifene Hydrochloride Raloxifene Hydrochloride TABLET, FILM COATED ORAL 20240123 N/A ANDA ANDA204310 A-S Medication Solutions RALOXIFENE HYDROCHLORIDE 60 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-7073-1)
43353-253-60 43353-253 HUMAN PRESCRIPTION DRUG Raloxifene Hydrochloride Raloxifene Hydrochloride TABLET, FILM COATED ORAL 20161115 N/A ANDA ANDA204310 Aphena Pharma Solutions - Tennessee, LLC RALOXIFENE HYDROCHLORIDE 60 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (43353-253-60)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase