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=ANDA077031"
符合检索条件的记录共 68 条，共 4 页，当前第 2 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
65862-006-01 65862-006 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20041028 N/A ANDA ANDA077031 Aurobindo Pharma Limited CITALOPRAM HYDROBROMIDE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-006-01)
65862-006-05 65862-006 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20041028 N/A ANDA ANDA077031 Aurobindo Pharma Limited CITALOPRAM HYDROBROMIDE 20 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-006-05)
65862-006-10 65862-006 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20041028 N/A ANDA ANDA077031 Aurobindo Pharma Limited CITALOPRAM HYDROBROMIDE 20 mg/1 10 BLISTER PACK in 1 CARTON (65862-006-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
65862-006-30 65862-006 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20041028 N/A ANDA ANDA077031 Aurobindo Pharma Limited CITALOPRAM HYDROBROMIDE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-006-30)
65862-006-32 65862-006 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20041028 N/A ANDA ANDA077031 Aurobindo Pharma Limited CITALOPRAM HYDROBROMIDE 20 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (65862-006-32)
65862-006-60 65862-006 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20041028 N/A ANDA ANDA077031 Aurobindo Pharma Limited CITALOPRAM HYDROBROMIDE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (65862-006-60)
65862-006-90 65862-006 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20041028 N/A ANDA ANDA077031 Aurobindo Pharma Limited CITALOPRAM HYDROBROMIDE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65862-006-90)
80425-0309-1 80425-0309 HUMAN PRESCRIPTION DRUG Citalopram Hydrobromide Citalopram Hydrobromide TABLET, FILM COATED ORAL 20230406 N/A ANDA ANDA077031 Advanced Rx Pharmacy of Tennessee, LLC CITALOPRAM HYDROBROMIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (80425-0309-1)
80425-0309-2 80425-0309 HUMAN PRESCRIPTION DRUG Citalopram Hydrobromide Citalopram Hydrobromide TABLET, FILM COATED ORAL 20230406 N/A ANDA ANDA077031 Advanced Rx Pharmacy of Tennessee, LLC CITALOPRAM HYDROBROMIDE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (80425-0309-2)
80425-0309-3 80425-0309 HUMAN PRESCRIPTION DRUG Citalopram Hydrobromide Citalopram Hydrobromide TABLET, FILM COATED ORAL 20230406 N/A ANDA ANDA077031 Advanced Rx Pharmacy of Tennessee, LLC CITALOPRAM HYDROBROMIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (80425-0309-3)
65862-007-01 65862-007 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20041028 N/A ANDA ANDA077031 Aurobindo Pharma Limited CITALOPRAM HYDROBROMIDE 40 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-007-01)
65862-007-05 65862-007 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20041028 N/A ANDA ANDA077031 Aurobindo Pharma Limited CITALOPRAM HYDROBROMIDE 40 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-007-05)
65862-007-10 65862-007 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20041028 N/A ANDA ANDA077031 Aurobindo Pharma Limited CITALOPRAM HYDROBROMIDE 40 mg/1 10 BLISTER PACK in 1 CARTON (65862-007-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
65862-007-30 65862-007 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20041028 N/A ANDA ANDA077031 Aurobindo Pharma Limited CITALOPRAM HYDROBROMIDE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-007-30)
65862-007-32 65862-007 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20041028 N/A ANDA ANDA077031 Aurobindo Pharma Limited CITALOPRAM HYDROBROMIDE 40 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (65862-007-32)
65862-007-60 65862-007 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20041028 N/A ANDA ANDA077031 Aurobindo Pharma Limited CITALOPRAM HYDROBROMIDE 40 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (65862-007-60)
65862-007-90 65862-007 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20041028 N/A ANDA ANDA077031 Aurobindo Pharma Limited CITALOPRAM HYDROBROMIDE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65862-007-90)
70518-4334-0 70518-4334 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20250428 N/A ANDA ANDA077031 REMEDYREPACK INC. CITALOPRAM HYDROBROMIDE 40 mg/1 100 POUCH in 1 BOX (70518-4334-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4334-1)
50090-3136-0 50090-3136 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20170913 N/A ANDA ANDA077031 A-S Medication Solutions CITALOPRAM HYDROBROMIDE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-3136-0)
50090-3136-1 50090-3136 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20240212 N/A ANDA ANDA077031 A-S Medication Solutions CITALOPRAM HYDROBROMIDE 40 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (50090-3136-1)
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