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
69097-822-15	69097-822	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET	ORAL	20160722	N/A	ANDA	ANDA077534	Cipla USA Inc.	CITALOPRAM HYDROBROMIDE	10 mg/1	1000 TABLET in 1 BOTTLE (69097-822-15)
69097-823-02	69097-823	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET	ORAL	20160722	N/A	ANDA	ANDA077534	Cipla USA Inc.	CITALOPRAM HYDROBROMIDE	20 mg/1	30 TABLET in 1 BOTTLE (69097-823-02)
69097-823-07	69097-823	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET	ORAL	20160722	N/A	ANDA	ANDA077534	Cipla USA Inc.	CITALOPRAM HYDROBROMIDE	20 mg/1	100 TABLET in 1 BOTTLE (69097-823-07)
69097-823-12	69097-823	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET	ORAL	20160722	N/A	ANDA	ANDA077534	Cipla USA Inc.	CITALOPRAM HYDROBROMIDE	20 mg/1	500 TABLET in 1 BOTTLE (69097-823-12)
69097-823-15	69097-823	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET	ORAL	20160722	N/A	ANDA	ANDA077534	Cipla USA Inc.	CITALOPRAM HYDROBROMIDE	20 mg/1	1000 TABLET in 1 BOTTLE (69097-823-15)
69097-824-02	69097-824	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET	ORAL	20160722	N/A	ANDA	ANDA077534	Cipla USA Inc.	CITALOPRAM HYDROBROMIDE	40 mg/1	30 TABLET in 1 BOTTLE (69097-824-02)
69097-824-07	69097-824	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET	ORAL	20160722	N/A	ANDA	ANDA077534	Cipla USA Inc.	CITALOPRAM HYDROBROMIDE	40 mg/1	100 TABLET in 1 BOTTLE (69097-824-07)
69097-824-12	69097-824	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET	ORAL	20160722	N/A	ANDA	ANDA077534	Cipla USA Inc.	CITALOPRAM HYDROBROMIDE	40 mg/1	500 TABLET in 1 BOTTLE (69097-824-12)
69097-824-15	69097-824	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET	ORAL	20160722	N/A	ANDA	ANDA077534	Cipla USA Inc.	CITALOPRAM HYDROBROMIDE	40 mg/1	1000 TABLET in 1 BOTTLE (69097-824-15)
69097-822-12	69097-822	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET	ORAL	20160722	N/A	ANDA	ANDA077534	Cipla USA Inc.	CITALOPRAM HYDROBROMIDE	10 mg/1	500 TABLET in 1 BOTTLE (69097-822-12)
69097-822-07	69097-822	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET	ORAL	20160722	N/A	ANDA	ANDA077534	Cipla USA Inc.	CITALOPRAM HYDROBROMIDE	10 mg/1	100 TABLET in 1 BOTTLE (69097-822-07)
69097-822-02	69097-822	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET	ORAL	20160722	N/A	ANDA	ANDA077534	Cipla USA Inc.	CITALOPRAM HYDROBROMIDE	10 mg/1	30 TABLET in 1 BOTTLE (69097-822-02)
50090-5170-0	50090-5170	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET	ORAL	20200925	N/A	ANDA	ANDA077534	A-S Medication Solutions	CITALOPRAM HYDROBROMIDE	10 mg/1	100 TABLET in 1 BOTTLE (50090-5170-0)
50090-5172-1	50090-5172	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET	ORAL	20200925	N/A	ANDA	ANDA077534	A-S Medication Solutions	CITALOPRAM HYDROBROMIDE	20 mg/1	60 TABLET in 1 BOTTLE (50090-5172-1)
50090-5172-2	50090-5172	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET	ORAL	20200925	N/A	ANDA	ANDA077534	A-S Medication Solutions	CITALOPRAM HYDROBROMIDE	20 mg/1	100 TABLET in 1 BOTTLE (50090-5172-2)
50090-5172-3	50090-5172	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET	ORAL	20200925	N/A	ANDA	ANDA077534	A-S Medication Solutions	CITALOPRAM HYDROBROMIDE	20 mg/1	90 TABLET in 1 BOTTLE (50090-5172-3)
50090-5175-0	50090-5175	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET	ORAL	20200925	N/A	ANDA	ANDA077534	A-S Medication Solutions	CITALOPRAM HYDROBROMIDE	40 mg/1	30 TABLET in 1 BOTTLE (50090-5175-0)
50090-5175-1	50090-5175	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET	ORAL	20200925	N/A	ANDA	ANDA077534	A-S Medication Solutions	CITALOPRAM HYDROBROMIDE	40 mg/1	100 TABLET in 1 BOTTLE (50090-5175-1)
50090-5175-2	50090-5175	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET	ORAL	20200925	N/A	ANDA	ANDA077534	A-S Medication Solutions	CITALOPRAM HYDROBROMIDE	40 mg/1	90 TABLET in 1 BOTTLE (50090-5175-2)
50090-5170-1	50090-5170	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET	ORAL	20200925	N/A	ANDA	ANDA077534	A-S Medication Solutions	CITALOPRAM HYDROBROMIDE	10 mg/1	30 TABLET in 1 BOTTLE (50090-5170-1)