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=ANDA077206"
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
51655-173-52 51655-173 HUMAN PRESCRIPTION DRUG Sertraline Hydrochloride Sertraline Hydrochloride TABLET, FILM COATED ORAL 20200617 N/A ANDA ANDA077206 Northwind Pharmaceuticals, LLC SERTRALINE HYDROCHLORIDE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-173-52)
50090-6379-1 50090-6379 HUMAN PRESCRIPTION DRUG Sertraline Hydrochloride Sertraline Hydrochloride TABLET, FILM COATED ORAL 20230223 N/A ANDA ANDA077206 A-S Medication Solutions SERTRALINE HYDROCHLORIDE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-6379-1)
50090-6379-2 50090-6379 HUMAN PRESCRIPTION DRUG Sertraline Hydrochloride Sertraline Hydrochloride TABLET, FILM COATED ORAL 20230223 N/A ANDA ANDA077206 A-S Medication Solutions SERTRALINE HYDROCHLORIDE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6379-2)
51655-265-26 51655-265 HUMAN PRESCRIPTION DRUG Sertraline Hydrochloride Sertraline Hydrochloride TABLET, FILM COATED ORAL 20200608 N/A ANDA ANDA077206 Northwind Pharmaceuticals, LLC SERTRALINE HYDROCHLORIDE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-265-26)
50090-6614-0 50090-6614 HUMAN PRESCRIPTION DRUG Sertraline Hydrochloride Sertraline Hydrochloride TABLET, FILM COATED ORAL 20230824 N/A ANDA ANDA077206 A-S Medication Solutions SERTRALINE HYDROCHLORIDE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6614-0)
65862-011-30 65862-011 HUMAN PRESCRIPTION DRUG Sertraline Hydrochloride Sertraline Hydrochloride TABLET, FILM COATED ORAL 20070206 N/A ANDA ANDA077206 Aurobindo Pharma Limited SERTRALINE HYDROCHLORIDE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-011-30)
65862-011-51 65862-011 HUMAN PRESCRIPTION DRUG Sertraline Hydrochloride Sertraline Hydrochloride TABLET, FILM COATED ORAL 20070206 N/A ANDA ANDA077206 Aurobindo Pharma Limited SERTRALINE HYDROCHLORIDE 25 mg/1 5000 TABLET, FILM COATED in 1 BOTTLE (65862-011-51)
65862-011-60 65862-011 HUMAN PRESCRIPTION DRUG Sertraline Hydrochloride Sertraline Hydrochloride TABLET, FILM COATED ORAL 20070206 N/A ANDA ANDA077206 Aurobindo Pharma Limited SERTRALINE HYDROCHLORIDE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (65862-011-60)
65862-011-90 65862-011 HUMAN PRESCRIPTION DRUG Sertraline Hydrochloride Sertraline Hydrochloride TABLET, FILM COATED ORAL 20070206 N/A ANDA ANDA077206 Aurobindo Pharma Limited SERTRALINE HYDROCHLORIDE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65862-011-90)
65862-011-99 65862-011 HUMAN PRESCRIPTION DRUG Sertraline Hydrochloride Sertraline Hydrochloride TABLET, FILM COATED ORAL 20070206 N/A ANDA ANDA077206 Aurobindo Pharma Limited SERTRALINE HYDROCHLORIDE 25 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65862-011-99)
65862-012-01 65862-012 HUMAN PRESCRIPTION DRUG Sertraline Hydrochloride Sertraline Hydrochloride TABLET, FILM COATED ORAL 20070206 N/A ANDA ANDA077206 Aurobindo Pharma Limited SERTRALINE HYDROCHLORIDE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-012-01)
65862-012-05 65862-012 HUMAN PRESCRIPTION DRUG Sertraline Hydrochloride Sertraline Hydrochloride TABLET, FILM COATED ORAL 20070206 N/A ANDA ANDA077206 Aurobindo Pharma Limited SERTRALINE HYDROCHLORIDE 50 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-012-05)
65862-012-30 65862-012 HUMAN PRESCRIPTION DRUG Sertraline Hydrochloride Sertraline Hydrochloride TABLET, FILM COATED ORAL 20070206 N/A ANDA ANDA077206 Aurobindo Pharma Limited SERTRALINE HYDROCHLORIDE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-012-30)
65862-012-50 65862-012 HUMAN PRESCRIPTION DRUG Sertraline Hydrochloride Sertraline Hydrochloride TABLET, FILM COATED ORAL 20070206 N/A ANDA ANDA077206 Aurobindo Pharma Limited SERTRALINE HYDROCHLORIDE 50 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (65862-012-50)
65862-012-51 65862-012 HUMAN PRESCRIPTION DRUG Sertraline Hydrochloride Sertraline Hydrochloride TABLET, FILM COATED ORAL 20070206 N/A ANDA ANDA077206 Aurobindo Pharma Limited SERTRALINE HYDROCHLORIDE 50 mg/1 5000 TABLET, FILM COATED in 1 BOTTLE (65862-012-51)
65862-012-60 65862-012 HUMAN PRESCRIPTION DRUG Sertraline Hydrochloride Sertraline Hydrochloride TABLET, FILM COATED ORAL 20070206 N/A ANDA ANDA077206 Aurobindo Pharma Limited SERTRALINE HYDROCHLORIDE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (65862-012-60)
65862-012-90 65862-012 HUMAN PRESCRIPTION DRUG Sertraline Hydrochloride Sertraline Hydrochloride TABLET, FILM COATED ORAL 20070206 N/A ANDA ANDA077206 Aurobindo Pharma Limited SERTRALINE HYDROCHLORIDE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65862-012-90)
65862-012-99 65862-012 HUMAN PRESCRIPTION DRUG Sertraline Hydrochloride Sertraline Hydrochloride TABLET, FILM COATED ORAL 20070206 N/A ANDA ANDA077206 Aurobindo Pharma Limited SERTRALINE HYDROCHLORIDE 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65862-012-99)
65862-013-01 65862-013 HUMAN PRESCRIPTION DRUG Sertraline Hydrochloride Sertraline Hydrochloride TABLET, FILM COATED ORAL 20070206 N/A ANDA ANDA077206 Aurobindo Pharma Limited SERTRALINE HYDROCHLORIDE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-013-01)
65862-013-05 65862-013 HUMAN PRESCRIPTION DRUG Sertraline Hydrochloride Sertraline Hydrochloride TABLET, FILM COATED ORAL 20070206 N/A ANDA ANDA077206 Aurobindo Pharma Limited SERTRALINE HYDROCHLORIDE 100 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-013-05)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase