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
13668-009-01	13668-009	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET, FILM COATED	ORAL	20071018	N/A	ANDA	ANDA078216	Torrent Pharmaceuticals Limited	CITALOPRAM HYDROBROMIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (13668-009-01)
13668-009-05	13668-009	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET, FILM COATED	ORAL	20071018	N/A	ANDA	ANDA078216	Torrent Pharmaceuticals Limited	CITALOPRAM HYDROBROMIDE	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (13668-009-05)
13668-009-09	13668-009	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET, FILM COATED	ORAL	20071018	N/A	ANDA	ANDA078216	Torrent Pharmaceuticals Limited	CITALOPRAM HYDROBROMIDE	10 mg/1	9990 TABLET, FILM COATED in 1 BOTTLE (13668-009-09)
13668-009-30	13668-009	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET, FILM COATED	ORAL	20071018	N/A	ANDA	ANDA078216	Torrent Pharmaceuticals Limited	CITALOPRAM HYDROBROMIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (13668-009-30)
13668-010-01	13668-010	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET, FILM COATED	ORAL	20071018	N/A	ANDA	ANDA078216	Torrent Pharmaceuticals Limited	CITALOPRAM HYDROBROMIDE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (13668-010-01)
13668-010-05	13668-010	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET, FILM COATED	ORAL	20071018	N/A	ANDA	ANDA078216	Torrent Pharmaceuticals Limited	CITALOPRAM HYDROBROMIDE	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (13668-010-05)
13668-010-06	13668-010	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET, FILM COATED	ORAL	20071018	N/A	ANDA	ANDA078216	Torrent Pharmaceuticals Limited	CITALOPRAM HYDROBROMIDE	20 mg/1	5600 TABLET, FILM COATED in 1 BOTTLE (13668-010-06)
13668-010-30	13668-010	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET, FILM COATED	ORAL	20071018	N/A	ANDA	ANDA078216	Torrent Pharmaceuticals Limited	CITALOPRAM HYDROBROMIDE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (13668-010-30)
13668-011-01	13668-011	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET, FILM COATED	ORAL	20071018	N/A	ANDA	ANDA078216	Torrent Pharmaceuticals Limited	CITALOPRAM HYDROBROMIDE	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (13668-011-01)
13668-011-05	13668-011	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET, FILM COATED	ORAL	20071018	N/A	ANDA	ANDA078216	Torrent Pharmaceuticals Limited	CITALOPRAM HYDROBROMIDE	40 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (13668-011-05)
13668-011-08	13668-011	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET, FILM COATED	ORAL	20071018	N/A	ANDA	ANDA078216	Torrent Pharmaceuticals Limited	CITALOPRAM HYDROBROMIDE	40 mg/1	2800 TABLET, FILM COATED in 1 BOTTLE (13668-011-08)
13668-011-30	13668-011	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET, FILM COATED	ORAL	20071018	N/A	ANDA	ANDA078216	Torrent Pharmaceuticals Limited	CITALOPRAM HYDROBROMIDE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (13668-011-30)
71205-764-30	71205-764	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET	ORAL	20230214	N/A	ANDA	ANDA078216	Proficient Rx LP	CITALOPRAM HYDROBROMIDE	40 mg/1	30 TABLET in 1 BOTTLE (71205-764-30)
71205-764-60	71205-764	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET	ORAL	20230214	N/A	ANDA	ANDA078216	Proficient Rx LP	CITALOPRAM HYDROBROMIDE	40 mg/1	60 TABLET in 1 BOTTLE (71205-764-60)
71205-764-90	71205-764	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET	ORAL	20230214	N/A	ANDA	ANDA078216	Proficient Rx LP	CITALOPRAM HYDROBROMIDE	40 mg/1	90 TABLET in 1 BOTTLE (71205-764-90)
55700-787-30	55700-787	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET	ORAL	20190830	20270930	ANDA	ANDA078216	Quality Care Products, LLC	CITALOPRAM HYDROBROMIDE	10 mg/1	30 TABLET in 1 BOTTLE (55700-787-30)
55700-787-90	55700-787	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET	ORAL	20190830	20270930	ANDA	ANDA078216	Quality Care Products, LLC	CITALOPRAM HYDROBROMIDE	10 mg/1	90 TABLET in 1 BOTTLE (55700-787-90)
55700-851-90	55700-851	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET	ORAL	20200820	20261031	ANDA	ANDA078216	Quality Care Products, LLC	CITALOPRAM HYDROBROMIDE	20 mg/1	90 TABLET in 1 BOTTLE (55700-851-90)
70518-4335-0	70518-4335	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET, FILM COATED	ORAL	20250501	N/A	ANDA	ANDA078216	REMEDYREPACK INC.	CITALOPRAM HYDROBROMIDE	20 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4335-0)
70518-4335-1	70518-4335	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET, FILM COATED	ORAL	20250601	N/A	ANDA	ANDA078216	REMEDYREPACK INC.	CITALOPRAM HYDROBROMIDE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4335-1)