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
63187-140-30 63187-140 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20181201 N/A ANDA ANDA077031 Proficient Rx LP CITALOPRAM HYDROBROMIDE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63187-140-30)
63187-140-60 63187-140 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20181201 N/A ANDA ANDA077031 Proficient Rx LP CITALOPRAM HYDROBROMIDE 40 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63187-140-60)
63187-140-90 63187-140 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20181201 N/A ANDA ANDA077031 Proficient Rx LP CITALOPRAM HYDROBROMIDE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63187-140-90)
53002-1359-0 53002-1359 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20170901 N/A ANDA ANDA077031 RPK Pharmaceuticals, Inc. CITALOPRAM HYDROBROMIDE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (53002-1359-0)
53002-1359-3 53002-1359 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20170901 N/A ANDA ANDA077031 RPK Pharmaceuticals, Inc. CITALOPRAM HYDROBROMIDE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (53002-1359-3)
53002-1359-6 53002-1359 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20170901 N/A ANDA ANDA077031 RPK Pharmaceuticals, Inc. CITALOPRAM HYDROBROMIDE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (53002-1359-6)
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)
51655-605-26 51655-605 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20220302 N/A ANDA ANDA077031 Northwind Pharmaceuticals 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 Pharmaceuticals CITALOPRAM HYDROBROMIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-605-52)
63187-679-00 63187-679 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20160401 N/A ANDA ANDA077031 Proficient Rx LP CITALOPRAM HYDROBROMIDE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (63187-679-00)
63187-679-30 63187-679 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20160401 N/A ANDA ANDA077031 Proficient Rx LP CITALOPRAM HYDROBROMIDE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63187-679-30)
63187-679-60 63187-679 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20160401 N/A ANDA ANDA077031 Proficient Rx LP CITALOPRAM HYDROBROMIDE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63187-679-60)
63187-679-90 63187-679 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20160401 N/A ANDA ANDA077031 Proficient Rx LP CITALOPRAM HYDROBROMIDE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63187-679-90)
68084-737-01 68084-737 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20140318 20240930 ANDA ANDA077031 American Health Packaging CITALOPRAM HYDROBROMIDE 10 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-737-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-737-11)
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)
51655-680-52 51655-680 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20220302 N/A ANDA ANDA077031 Northwind Pharmaceuticals CITALOPRAM HYDROBROMIDE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-680-52)
51655-680-26 51655-680 HUMAN PRESCRIPTION DRUG Citalopram Citalopram Hydrobromide TABLET, FILM COATED ORAL 20220504 N/A ANDA ANDA077031 Northwind Pharmaceuticals CITALOPRAM HYDROBROMIDE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-680-26)
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)
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