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
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)
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)
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)