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 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
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)
65862-005-01 65862-005 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20041028 N/A ANDA ANDA077031 Aurobindo Pharma Limited CITALOPRAM HYDROBROMIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-005-01)
65862-005-05 65862-005 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20041028 N/A ANDA ANDA077031 Aurobindo Pharma Limited CITALOPRAM HYDROBROMIDE 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-005-05)
65862-005-10 65862-005 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20041028 N/A ANDA ANDA077031 Aurobindo Pharma Limited CITALOPRAM HYDROBROMIDE 10 mg/1 10 BLISTER PACK in 1 CARTON (65862-005-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
65862-005-30 65862-005 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20041028 N/A ANDA ANDA077031 Aurobindo Pharma Limited CITALOPRAM HYDROBROMIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-005-30)
65862-005-32 65862-005 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20041028 N/A ANDA ANDA077031 Aurobindo Pharma Limited CITALOPRAM HYDROBROMIDE 10 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (65862-005-32)
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)
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)
82009-108-05 82009-108 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20230801 N/A ANDA ANDA077031 QUALLENT PHARMACEUTICALS HEALTH LLC CITALOPRAM HYDROBROMIDE 40 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (82009-108-05)
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)
65862-005-60 65862-005 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20041028 N/A ANDA ANDA077031 Aurobindo Pharma Limited CITALOPRAM HYDROBROMIDE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (65862-005-60)
65862-005-90 65862-005 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20041028 N/A ANDA ANDA077031 Aurobindo Pharma Limited CITALOPRAM HYDROBROMIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65862-005-90)
51655-605-26 51655-605 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20220302 N/A ANDA ANDA077031 Northwind Health Company, LLC CITALOPRAM HYDROBROMIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-605-26)
51655-605-52 51655-605 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20210401 N/A ANDA ANDA077031 Northwind Health Company, LLC CITALOPRAM HYDROBROMIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-605-52)
50090-6433-0 50090-6433 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20230411 N/A ANDA ANDA077031 A-S Medication Solutions CITALOPRAM HYDROBROMIDE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-6433-0)
50090-6433-1 50090-6433 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20230411 N/A ANDA ANDA077031 A-S Medication Solutions CITALOPRAM HYDROBROMIDE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-6433-1)
50090-6433-2 50090-6433 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20230411 N/A ANDA ANDA077031 A-S Medication Solutions CITALOPRAM HYDROBROMIDE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (50090-6433-2)
50090-6433-3 50090-6433 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20230417 N/A ANDA ANDA077031 A-S Medication Solutions CITALOPRAM HYDROBROMIDE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6433-3)
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