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=ANDA090432"
符合检索条件的记录共 67 条，共 4 页，当前第 2 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
65862-374-59 65862-374 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20120911 N/A ANDA ANDA090432 Aurobindo Pharma Limited ESCITALOPRAM OXALATE 10 mg/1 5000 TABLET, FILM COATED in 1 BOTTLE (65862-374-59)
65862-374-90 65862-374 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20120911 N/A ANDA ANDA090432 Aurobindo Pharma Limited ESCITALOPRAM OXALATE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65862-374-90)
65862-375-01 65862-375 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20120911 N/A ANDA ANDA090432 Aurobindo Pharma Limited ESCITALOPRAM OXALATE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-375-01)
65862-375-05 65862-375 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20120911 N/A ANDA ANDA090432 Aurobindo Pharma Limited ESCITALOPRAM OXALATE 20 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-375-05)
65862-375-10 65862-375 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20120911 N/A ANDA ANDA090432 Aurobindo Pharma Limited ESCITALOPRAM OXALATE 20 mg/1 10 BLISTER PACK in 1 CARTON (65862-375-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
65862-375-30 65862-375 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20120911 N/A ANDA ANDA090432 Aurobindo Pharma Limited ESCITALOPRAM OXALATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-375-30)
65862-375-39 65862-375 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20120911 N/A ANDA ANDA090432 Aurobindo Pharma Limited ESCITALOPRAM OXALATE 20 mg/1 3000 TABLET, FILM COATED in 1 BOTTLE (65862-375-39)
65862-375-90 65862-375 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20120911 N/A ANDA ANDA090432 Aurobindo Pharma Limited ESCITALOPRAM OXALATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65862-375-90)
76420-721-01 76420-721 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA090432 Asclemed USA, Inc. ESCITALOPRAM OXALATE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-721-01)
76420-721-05 76420-721 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA090432 Asclemed USA, Inc. ESCITALOPRAM OXALATE 5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76420-721-05)
76420-721-10 76420-721 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA090432 Asclemed USA, Inc. ESCITALOPRAM OXALATE 5 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (76420-721-10)
76420-721-30 76420-721 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA090432 Asclemed USA, Inc. ESCITALOPRAM OXALATE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-721-30)
76420-721-60 76420-721 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA090432 Asclemed USA, Inc. ESCITALOPRAM OXALATE 5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-721-60)
76420-721-90 76420-721 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA090432 Asclemed USA, Inc. ESCITALOPRAM OXALATE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-721-90)
76420-722-01 76420-722 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA090432 Asclemed USA, Inc. ESCITALOPRAM OXALATE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-722-01)
76420-722-05 76420-722 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA090432 Asclemed USA, Inc. ESCITALOPRAM OXALATE 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76420-722-05)
76420-722-10 76420-722 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA090432 Asclemed USA, Inc. ESCITALOPRAM OXALATE 10 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (76420-722-10)
76420-722-30 76420-722 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA090432 Asclemed USA, Inc. ESCITALOPRAM OXALATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-722-30)
76420-722-60 76420-722 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA090432 Asclemed USA, Inc. ESCITALOPRAM OXALATE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-722-60)
76420-722-90 76420-722 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA090432 Asclemed USA, Inc. ESCITALOPRAM OXALATE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-722-90)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase