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"
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
51655-147-26 51655-147 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20230125 N/A ANDA ANDA090432 Northwind Pharmaceuticals, LLC ESCITALOPRAM OXALATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-147-26)
71335-9687-1 71335-9687 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20230622 N/A ANDA ANDA090432 Bryant Ranch Prepack ESCITALOPRAM OXALATE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-9687-1)
71335-9687-2 71335-9687 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20230404 N/A ANDA ANDA090432 Bryant Ranch Prepack ESCITALOPRAM OXALATE 5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-9687-2)
71335-9687-3 71335-9687 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20230710 N/A ANDA ANDA090432 Bryant Ranch Prepack ESCITALOPRAM OXALATE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-9687-3)
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)
65862-374-01 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)
53002-2431-0 53002-2431 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20240101 N/A ANDA ANDA090432 RPK Pharmaceuticals, Inc. ESCITALOPRAM OXALATE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (53002-2431-0)
53002-2431-3 53002-2431 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20240101 N/A ANDA ANDA090432 RPK Pharmaceuticals, Inc. ESCITALOPRAM OXALATE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (53002-2431-3)
68084-617-01 68084-617 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20121008 N/A ANDA ANDA090432 American Health Packaging ESCITALOPRAM OXALATE 10 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-617-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-617-11)
71205-193-30 71205-193 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20190101 N/A ANDA ANDA090432 Proficient Rx LP ESCITALOPRAM OXALATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-193-30)
71205-193-60 71205-193 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20190101 N/A ANDA ANDA090432 Proficient Rx LP ESCITALOPRAM OXALATE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-193-60)
71205-193-90 71205-193 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20190101 N/A ANDA ANDA090432 Proficient Rx LP ESCITALOPRAM OXALATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-193-90)
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
70518-1103-1 70518-1103 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20231208 N/A ANDA ANDA090432 REMEDYREPACK INC. ESCITALOPRAM OXALATE 10 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1103-1)
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