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 68 条，共 4 页，当前第 3 页 ，可点击列名称排序
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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
71335-9687-4 71335-9687 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20241101 N/A ANDA ANDA090432 Bryant Ranch Prepack ESCITALOPRAM OXALATE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-9687-4)
65862-373-01 65862-373 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20120911 N/A ANDA ANDA090432 Aurobindo Pharma Limited ESCITALOPRAM OXALATE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-373-01)
65862-373-05 65862-373 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20120911 N/A ANDA ANDA090432 Aurobindo Pharma Limited ESCITALOPRAM OXALATE 5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-373-05)
65862-373-10 65862-373 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20120911 N/A ANDA ANDA090432 Aurobindo Pharma Limited ESCITALOPRAM OXALATE 5 mg/1 10 BLISTER PACK in 1 CARTON (65862-373-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
65862-373-19 65862-373 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20120911 N/A ANDA ANDA090432 Aurobindo Pharma Limited ESCITALOPRAM OXALATE 5 mg/1 10000 TABLET, FILM COATED in 1 BOTTLE (65862-373-19)
65862-373-30 65862-373 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20120911 N/A ANDA ANDA090432 Aurobindo Pharma Limited ESCITALOPRAM OXALATE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-373-30)
65862-373-90 65862-373 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20120911 N/A ANDA ANDA090432 Aurobindo Pharma Limited ESCITALOPRAM OXALATE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65862-373-90)
65862-374-01 65862-374 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20120911 N/A ANDA ANDA090432 Aurobindo Pharma Limited ESCITALOPRAM OXALATE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-374-01)
65862-374-05 65862-374 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20120911 N/A ANDA ANDA090432 Aurobindo Pharma Limited ESCITALOPRAM OXALATE 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-374-05)
65862-374-10 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 10 BLISTER PACK in 1 CARTON (65862-374-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
65862-374-30 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 30 TABLET, FILM COATED in 1 BOTTLE (65862-374-30)
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)
70518-1103-0 70518-1103 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20180409 N/A ANDA ANDA090432 REMEDYREPACK INC. ESCITALOPRAM OXALATE 10 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1103-0)
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