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
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)
80425-0375-3 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 90 TABLET, FILM COATED in 1 BOTTLE (80425-0375-3)
76420-723-01 76420-723 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA090432 Asclemed USA, Inc. ESCITALOPRAM OXALATE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-723-01)
76420-723-05 76420-723 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA090432 Asclemed USA, Inc. ESCITALOPRAM OXALATE 20 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76420-723-05)
76420-723-10 76420-723 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA090432 Asclemed USA, Inc. ESCITALOPRAM OXALATE 20 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (76420-723-10)
76420-723-30 76420-723 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA090432 Asclemed USA, Inc. ESCITALOPRAM OXALATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-723-30)
76420-723-60 76420-723 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA090432 Asclemed USA, Inc. ESCITALOPRAM OXALATE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-723-60)
76420-723-90 76420-723 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram Oxalate TABLET, FILM COATED ORAL 20240506 N/A ANDA ANDA090432 Asclemed USA, Inc. ESCITALOPRAM OXALATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-723-90)
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)
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)
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)
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)
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)
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