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"
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
68071-3357-4 68071-3357 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20170714 N/A ANDA ANDA077031 NuCare Pharmaceuticals,Inc. CITALOPRAM HYDROBROMIDE 40 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (68071-3357-4)
68071-3357-5 68071-3357 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20170714 N/A ANDA ANDA077031 NuCare Pharmaceuticals,Inc. CITALOPRAM HYDROBROMIDE 40 mg/1 45 TABLET, FILM COATED in 1 BOTTLE (68071-3357-5)
68071-3357-6 68071-3357 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20170714 N/A ANDA ANDA077031 NuCare Pharmaceuticals,Inc. CITALOPRAM HYDROBROMIDE 40 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68071-3357-6)
68071-3357-9 68071-3357 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20170714 N/A ANDA ANDA077031 NuCare Pharmaceuticals,Inc. CITALOPRAM HYDROBROMIDE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-3357-9)
42708-019-30 42708-019 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20180314 N/A ANDA ANDA077031 QPharma, Inc. CITALOPRAM HYDROBROMIDE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (42708-019-30)
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)
65862-005-01 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)
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)
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)
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)
0615-8023-05 0615-8023 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 20 mg/1 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8023-05)
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)
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)
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)
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)
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