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
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)
42708-077-30 42708-077 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20181218 N/A ANDA ANDA090432 QPharma, Inc. ESCITALOPRAM OXALATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (42708-077-30)
51655-147-26 51655-147 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20230125 N/A ANDA ANDA090432 Northwind Health Company, LLC ESCITALOPRAM OXALATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-147-26)
0615-8475-05 0615-8475 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20230810 N/A ANDA ANDA090432 NCS HealthCare of KY, LLC dba Vangard Labs ESCITALOPRAM OXALATE 5 mg/1 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8475-05)
0615-8475-39 0615-8475 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20230517 N/A ANDA ANDA090432 NCS HealthCare of KY, LLC dba Vangard Labs ESCITALOPRAM OXALATE 5 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8475-39)
0615-8476-05 0615-8476 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20230510 N/A ANDA ANDA090432 NCS HealthCare of KY, LLC dba Vangard Labs ESCITALOPRAM OXALATE 10 mg/1 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8476-05)
0615-8476-28 0615-8476 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20250115 N/A ANDA ANDA090432 NCS HealthCare of KY, LLC dba Vangard Labs ESCITALOPRAM OXALATE 10 mg/1 28 TABLET, FILM COATED in 1 BLISTER PACK (0615-8476-28)
0615-8476-39 0615-8476 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20230510 N/A ANDA ANDA090432 NCS HealthCare of KY, LLC dba Vangard Labs ESCITALOPRAM OXALATE 10 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8476-39)
0615-8477-05 0615-8477 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20230718 N/A ANDA ANDA090432 NCS HealthCare of KY, LLC dba Vangard Labs ESCITALOPRAM OXALATE 20 mg/1 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8477-05)
0615-8477-39 0615-8477 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20230718 N/A ANDA ANDA090432 NCS HealthCare of KY, LLC dba Vangard Labs ESCITALOPRAM OXALATE 20 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8477-39)
60760-590-90 60760-590 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20231024 N/A ANDA ANDA090432 ST. MARY'S MEDICAL PARK PHARMACY ESCITALOPRAM OXALATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-590-90)
50090-6023-0 50090-6023 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20220627 N/A ANDA ANDA090432 A-S Medication Solutions ESCITALOPRAM OXALATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-6023-0)
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