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
68071-3558-1	68071-3558	HUMAN PRESCRIPTION DRUG	Citalopram	citalopram	TABLET, FILM COATED	ORAL	20240102	N/A	ANDA	ANDA077042	NuCare Pharmaceuticals,Inc.	CITALOPRAM HYDROBROMIDE	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3558-1)
0378-6231-01	0378-6231	HUMAN PRESCRIPTION DRUG	Citalopram	citalopram	TABLET, FILM COATED	ORAL	20080728	N/A	ANDA	ANDA077042	Mylan Pharmaceuticals Inc.	CITALOPRAM HYDROBROMIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6231-01)
0378-6231-05	0378-6231	HUMAN PRESCRIPTION DRUG	Citalopram	citalopram	TABLET, FILM COATED	ORAL	20080728	N/A	ANDA	ANDA077042	Mylan Pharmaceuticals Inc.	CITALOPRAM HYDROBROMIDE	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6231-05)
70518-2601-3	70518-2601	HUMAN PRESCRIPTION DRUG	Citalopram	citalopram	TABLET, FILM COATED	ORAL	20240416	N/A	ANDA	ANDA077042	REMEDYREPACK INC.	CITALOPRAM HYDROBROMIDE	40 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2601-3)
0378-6232-01	0378-6232	HUMAN PRESCRIPTION DRUG	Citalopram	citalopram	TABLET, FILM COATED	ORAL	20080728	N/A	ANDA	ANDA077042	Mylan Pharmaceuticals Inc.	CITALOPRAM HYDROBROMIDE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6232-01)
0378-6232-05	0378-6232	HUMAN PRESCRIPTION DRUG	Citalopram	citalopram	TABLET, FILM COATED	ORAL	20080728	N/A	ANDA	ANDA077042	Mylan Pharmaceuticals Inc.	CITALOPRAM HYDROBROMIDE	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6232-05)
0378-6233-01	0378-6233	HUMAN PRESCRIPTION DRUG	Citalopram	citalopram	TABLET, FILM COATED	ORAL	20080728	N/A	ANDA	ANDA077042	Mylan Pharmaceuticals Inc.	CITALOPRAM HYDROBROMIDE	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6233-01)
0378-6233-05	0378-6233	HUMAN PRESCRIPTION DRUG	Citalopram	citalopram	TABLET, FILM COATED	ORAL	20080728	N/A	ANDA	ANDA077042	Mylan Pharmaceuticals Inc.	CITALOPRAM HYDROBROMIDE	40 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6233-05)
71335-2232-1	71335-2232	HUMAN PRESCRIPTION DRUG	Citalopram	citalopram	TABLET, FILM COATED	ORAL	20230918	N/A	ANDA	ANDA077042	Bryant Ranch Prepack	CITALOPRAM HYDROBROMIDE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-1)
71335-2232-2	71335-2232	HUMAN PRESCRIPTION DRUG	Citalopram	citalopram	TABLET, FILM COATED	ORAL	20241004	N/A	ANDA	ANDA077042	Bryant Ranch Prepack	CITALOPRAM HYDROBROMIDE	40 mg/1	40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-2)
71335-2232-3	71335-2232	HUMAN PRESCRIPTION DRUG	Citalopram	citalopram	TABLET, FILM COATED	ORAL	20241004	N/A	ANDA	ANDA077042	Bryant Ranch Prepack	CITALOPRAM HYDROBROMIDE	40 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-3)
71335-2232-4	71335-2232	HUMAN PRESCRIPTION DRUG	Citalopram	citalopram	TABLET, FILM COATED	ORAL	20230918	N/A	ANDA	ANDA077042	Bryant Ranch Prepack	CITALOPRAM HYDROBROMIDE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-4)
71335-2232-5	71335-2232	HUMAN PRESCRIPTION DRUG	Citalopram	citalopram	TABLET, FILM COATED	ORAL	20241004	N/A	ANDA	ANDA077042	Bryant Ranch Prepack	CITALOPRAM HYDROBROMIDE	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-5)
71335-2232-6	71335-2232	HUMAN PRESCRIPTION DRUG	Citalopram	citalopram	TABLET, FILM COATED	ORAL	20241004	N/A	ANDA	ANDA077042	Bryant Ranch Prepack	CITALOPRAM HYDROBROMIDE	40 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-6)