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）

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
80425-0309-1	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	30 TABLET, FILM COATED in 1 BOTTLE (80425-0309-1)
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)
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)
82009-107-05	82009-107	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram Hydrobromide	TABLET, FILM COATED	ORAL	20230801	N/A	ANDA	ANDA077031	QUALLENT PHARMACEUTICALS HEALTH LLC	CITALOPRAM HYDROBROMIDE	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (82009-107-05)
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)
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)
50090-7039-0	50090-7039	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram Hydrobromide	TABLET, FILM COATED	ORAL	20240111	N/A	ANDA	ANDA077031	A-S Medication Solutions	CITALOPRAM HYDROBROMIDE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-7039-0)
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)
65862-005-01	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)
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)