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
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)
70518-4334-0	70518-4334	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram Hydrobromide	TABLET, FILM COATED	ORAL	20250428	N/A	ANDA	ANDA077031	REMEDYREPACK INC.	CITALOPRAM HYDROBROMIDE	40 mg/1	100 POUCH in 1 BOX (70518-4334-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4334-1)
50090-3136-2	50090-3136	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram Hydrobromide	TABLET, FILM COATED	ORAL	20180822	N/A	ANDA	ANDA077031	A-S Medication Solutions	CITALOPRAM HYDROBROMIDE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-3136-2)
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)