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 65 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
0615-8022-05 0615-8022 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20041028 N/A ANDA ANDA077031 NCS HealthCare of KY, LLC dba Vangard Labs CITALOPRAM HYDROBROMIDE 10 mg/1 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8022-05)
43063-670-30 43063-670 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20160429 N/A ANDA ANDA077031 PD-Rx Pharmaceuticals, Inc. CITALOPRAM HYDROBROMIDE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-670-30)
43063-670-90 43063-670 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20160429 N/A ANDA ANDA077031 PD-Rx Pharmaceuticals, Inc. CITALOPRAM HYDROBROMIDE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-670-90)
53002-1360-0 53002-1360 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20170901 N/A ANDA ANDA077031 RPK Pharmaceuticals, Inc. CITALOPRAM HYDROBROMIDE 40 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (53002-1360-0)
53002-1360-3 53002-1360 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20170901 N/A ANDA ANDA077031 RPK Pharmaceuticals, Inc. CITALOPRAM HYDROBROMIDE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (53002-1360-3)
53002-1360-6 53002-1360 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20170901 N/A ANDA ANDA077031 RPK Pharmaceuticals, Inc. CITALOPRAM HYDROBROMIDE 40 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (53002-1360-6)
0615-8022-39 0615-8022 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20041028 N/A ANDA ANDA077031 NCS HealthCare of KY, LLC dba Vangard Labs CITALOPRAM HYDROBROMIDE 10 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8022-39)
82009-106-05 82009-106 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20230801 N/A ANDA ANDA077031 QUALLENT PHARMACEUTICALS HEALTH LLC CITALOPRAM HYDROBROMIDE 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (82009-106-05)
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)
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)
71610-413-60 71610-413 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20200403 N/A ANDA ANDA077031 Aphena Pharma Solutions - Tennessee, LLC CITALOPRAM HYDROBROMIDE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71610-413-60)
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