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=ANDA076921"
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
71610-115-60 71610-115 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20180809 N/A ANDA ANDA076921 Aphena Pharma Solutions - Tennessee, LLC MIRTAZAPINE 15 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71610-115-60)
0615-8269-39 0615-8269 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20190218 N/A ANDA ANDA076921 NCS HealthCare of KY, Inc dba Vangard Labs MIRTAZAPINE 30 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8269-39)
49999-629-30 49999-629 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20090817 N/A ANDA ANDA076921 Quality Care Products LLC MIRTAZAPINE 15 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (49999-629-30)
70518-0180-0 70518-0180 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20170126 N/A ANDA ANDA076921 REMEDYREPACK INC. MIRTAZAPINE 15 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0180-0)
49999-629-60 49999-629 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20090817 N/A ANDA ANDA076921 Quality Care Products LLC MIRTAZAPINE 15 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (49999-629-60)
0615-8489-05 0615-8489 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20230915 N/A ANDA ANDA076921 NCS HealthCare of KY, LLC dba Vangard Labs MIRTAZAPINE 7.5 mg/1 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8489-05)
0615-8489-39 0615-8489 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20230915 N/A ANDA ANDA076921 NCS HealthCare of KY, LLC dba Vangard Labs MIRTAZAPINE 7.5 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8489-39)
65862-001-01 65862-001 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20041022 N/A ANDA ANDA076921 Aurobindo Pharma Limited MIRTAZAPINE 7.5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-001-01)
65862-001-90 65862-001 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20041022 N/A ANDA ANDA076921 Aurobindo Pharma Limited MIRTAZAPINE 7.5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65862-001-90)
65862-001-05 65862-001 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20041022 N/A ANDA ANDA076921 Aurobindo Pharma Limited MIRTAZAPINE 7.5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-001-05)
65862-001-30 65862-001 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20041022 N/A ANDA ANDA076921 Aurobindo Pharma Limited MIRTAZAPINE 7.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-001-30)
65862-001-60 65862-001 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20041022 N/A ANDA ANDA076921 Aurobindo Pharma Limited MIRTAZAPINE 7.5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (65862-001-60)
65862-003-01 65862-003 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20041022 N/A ANDA ANDA076921 Aurobindo Pharma Limited MIRTAZAPINE 30 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-003-01)
65862-003-05 65862-003 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20041022 N/A ANDA ANDA076921 Aurobindo Pharma Limited MIRTAZAPINE 30 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-003-05)
65862-003-30 65862-003 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20041022 N/A ANDA ANDA076921 Aurobindo Pharma Limited MIRTAZAPINE 30 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-003-30)
65862-003-32 65862-003 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20041022 N/A ANDA ANDA076921 Aurobindo Pharma Limited MIRTAZAPINE 30 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (65862-003-32)
65862-003-60 65862-003 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20041022 N/A ANDA ANDA076921 Aurobindo Pharma Limited MIRTAZAPINE 30 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (65862-003-60)
65862-003-90 65862-003 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20041022 N/A ANDA ANDA076921 Aurobindo Pharma Limited MIRTAZAPINE 30 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65862-003-90)
71205-481-60 71205-481 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20201001 N/A ANDA ANDA076921 Proficient Rx LP MIRTAZAPINE 15 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-481-60)
71205-481-90 71205-481 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20201001 N/A ANDA ANDA076921 Proficient Rx LP MIRTAZAPINE 15 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-481-90)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase