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
50090-6846-0	50090-6846	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET	ORAL	20231129	N/A	ANDA	ANDA078216	A-S Medication Solutions	CITALOPRAM HYDROBROMIDE	20 mg/1	90 TABLET in 1 BOTTLE (50090-6846-0)
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)
70518-4335-2	70518-4335	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET, FILM COATED	ORAL	20250613	N/A	ANDA	ANDA078216	REMEDYREPACK INC.	CITALOPRAM HYDROBROMIDE	20 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4335-2)
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)
63187-220-00	63187-220	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET	ORAL	20151102	N/A	ANDA	ANDA078216	Proficient Rx LP	CITALOPRAM HYDROBROMIDE	10 mg/1	100 TABLET in 1 BOTTLE (63187-220-00)
63187-220-30	63187-220	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET	ORAL	20151102	N/A	ANDA	ANDA078216	Proficient Rx LP	CITALOPRAM HYDROBROMIDE	10 mg/1	30 TABLET in 1 BOTTLE (63187-220-30)
50090-6947-0	50090-6947	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET	ORAL	20231218	N/A	ANDA	ANDA078216	A-S Medication Solutions	CITALOPRAM HYDROBROMIDE	40 mg/1	90 TABLET in 1 BOTTLE (50090-6947-0)
70518-4416-0	70518-4416	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET, FILM COATED	ORAL	20250731	N/A	ANDA	ANDA078216	REMEDYREPACK INC.	CITALOPRAM HYDROBROMIDE	10 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4416-0)
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)
68071-2198-3	68071-2198	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET	ORAL	20170511	N/A	ANDA	ANDA078216	NuCare Pharmaceuticals, Inc.	CITALOPRAM HYDROBROMIDE	20 mg/1	30 TABLET in 1 BOTTLE (68071-2198-3)
68071-2198-6	68071-2198	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET	ORAL	20170511	N/A	ANDA	ANDA078216	NuCare Pharmaceuticals, Inc.	CITALOPRAM HYDROBROMIDE	20 mg/1	60 TABLET in 1 BOTTLE (68071-2198-6)
68071-2198-9	68071-2198	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET	ORAL	20170511	N/A	ANDA	ANDA078216	NuCare Pharmaceuticals, Inc.	CITALOPRAM HYDROBROMIDE	20 mg/1	90 TABLET in 1 BOTTLE (68071-2198-9)
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)