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 72 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
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)
70518-1103-1 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)
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)
68084-618-01 68084-618 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20121008 N/A ANDA ANDA090432 American Health Packaging ESCITALOPRAM OXALATE 20 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-618-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-618-11)
68071-2597-3 68071-2597 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20211214 N/A ANDA ANDA090432 NuCare Pharmaceuticals,Inc. ESCITALOPRAM OXALATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-2597-3)
68071-2597-9 68071-2597 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20211214 N/A ANDA ANDA090432 NuCare Pharmaceuticals,Inc. ESCITALOPRAM OXALATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-2597-9)
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)
80425-0375-1 80425-0375 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20240313 N/A ANDA ANDA090432 Advanced Rx Pharmacy of Tennessee, LLC ESCITALOPRAM OXALATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (80425-0375-1)
80425-0375-2 80425-0375 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20240313 N/A ANDA ANDA090432 Advanced Rx Pharmacy of Tennessee, LLC ESCITALOPRAM OXALATE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (80425-0375-2)
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