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
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)
0615-8141-39 0615-8141 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20180105 N/A ANDA ANDA077031 NCS HealthCare of KY, LLC dba Vangard Labs CITALOPRAM HYDROBROMIDE 40 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8141-39)
72162-2517-1 72162-2517 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20250609 N/A ANDA ANDA077031 Bryant Ranch Prepack CITALOPRAM HYDROBROMIDE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72162-2517-1)
72162-2517-5 72162-2517 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20250609 N/A ANDA ANDA077031 Bryant Ranch Prepack CITALOPRAM HYDROBROMIDE 20 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (72162-2517-5)
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)
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)
51655-680-26 51655-680 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20220504 N/A ANDA ANDA077031 Northwind Health Company, LLC CITALOPRAM HYDROBROMIDE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-680-26)
51655-680-52 51655-680 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20220302 N/A ANDA ANDA077031 Northwind Health Company, LLC CITALOPRAM HYDROBROMIDE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-680-52)
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)
65862-005-32 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)
65862-005-10 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)
65862-005-05 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)
65862-005-60 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)
65862-006-10 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)
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)
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