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
70518-0070-1	70518-0070	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET, FILM COATED	ORAL	20161229	20251231	ANDA	ANDA078216	REMEDYREPACK INC.	CITALOPRAM HYDROBROMIDE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70518-0070-1)
70518-0070-3	70518-0070	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET, FILM COATED	ORAL	20181106	20251231	ANDA	ANDA078216	REMEDYREPACK INC.	CITALOPRAM HYDROBROMIDE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0070-3)
68071-1830-1	68071-1830	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET	ORAL	20210624	N/A	ANDA	ANDA078216	NuCare Pharmaceuticals,Inc.	CITALOPRAM HYDROBROMIDE	20 mg/1	100 TABLET in 1 BOTTLE (68071-1830-1)
70518-0542-0	70518-0542	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET, FILM COATED	ORAL	20170517	20251231	ANDA	ANDA078216	REMEDYREPACK INC.	CITALOPRAM HYDROBROMIDE	10 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0542-0)
70518-0542-1	70518-0542	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET, FILM COATED	ORAL	20190425	20251231	ANDA	ANDA078216	REMEDYREPACK INC.	CITALOPRAM HYDROBROMIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0542-1)
68071-3384-1	68071-3384	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET	ORAL	20170718	N/A	ANDA	ANDA078216	NuCare Pharmaceuticals,Inc.	CITALOPRAM HYDROBROMIDE	40 mg/1	100 TABLET in 1 BOTTLE (68071-3384-1)
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)
71335-0238-2	71335-0238	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET	ORAL	20180919	N/A	ANDA	ANDA078216	Bryant Ranch Prepack	CITALOPRAM HYDROBROMIDE	20 mg/1	60 TABLET in 1 BOTTLE (71335-0238-2)
71335-0238-3	71335-0238	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET	ORAL	20180417	N/A	ANDA	ANDA078216	Bryant Ranch Prepack	CITALOPRAM HYDROBROMIDE	20 mg/1	90 TABLET in 1 BOTTLE (71335-0238-3)
71335-0238-4	71335-0238	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET	ORAL	20200624	N/A	ANDA	ANDA078216	Bryant Ranch Prepack	CITALOPRAM HYDROBROMIDE	20 mg/1	100 TABLET in 1 BOTTLE (71335-0238-4)
71335-0238-5	71335-0238	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET	ORAL	20241030	N/A	ANDA	ANDA078216	Bryant Ranch Prepack	CITALOPRAM HYDROBROMIDE	20 mg/1	15 TABLET in 1 BOTTLE (71335-0238-5)
71335-0238-6	71335-0238	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET	ORAL	20190905	N/A	ANDA	ANDA078216	Bryant Ranch Prepack	CITALOPRAM HYDROBROMIDE	20 mg/1	120 TABLET in 1 BOTTLE (71335-0238-6)
71335-0238-7	71335-0238	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET	ORAL	20241030	N/A	ANDA	ANDA078216	Bryant Ranch Prepack	CITALOPRAM HYDROBROMIDE	20 mg/1	7 TABLET in 1 BOTTLE (71335-0238-7)