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
71335-0480-5	71335-0480	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET	ORAL	20191111	N/A	ANDA	ANDA078216	Bryant Ranch Prepack	CITALOPRAM HYDROBROMIDE	40 mg/1	100 TABLET in 1 BOTTLE (71335-0480-5)
71335-0480-6	71335-0480	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET	ORAL	20230810	N/A	ANDA	ANDA078216	Bryant Ranch Prepack	CITALOPRAM HYDROBROMIDE	40 mg/1	180 TABLET in 1 BOTTLE (71335-0480-6)
72162-2567-1	72162-2567	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET, FILM COATED	ORAL	20251117	N/A	ANDA	ANDA078216	Bryant Ranch Prepack	CITALOPRAM HYDROBROMIDE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72162-2567-1)
72162-2567-5	72162-2567	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET, FILM COATED	ORAL	20251117	N/A	ANDA	ANDA078216	Bryant Ranch Prepack	CITALOPRAM HYDROBROMIDE	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72162-2567-5)
80425-0557-1	80425-0557	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET, FILM COATED	ORAL	20251107	N/A	ANDA	ANDA078216	Advanced Rx of Tennessee, LLC	CITALOPRAM HYDROBROMIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (80425-0557-1)
80425-0557-2	80425-0557	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET, FILM COATED	ORAL	20251107	N/A	ANDA	ANDA078216	Advanced Rx of Tennessee, LLC	CITALOPRAM HYDROBROMIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0557-2)
80425-0557-3	80425-0557	HUMAN PRESCRIPTION DRUG	Citalopram	Citalopram	TABLET, FILM COATED	ORAL	20251107	N/A	ANDA	ANDA078216	Advanced Rx of Tennessee, LLC	CITALOPRAM HYDROBROMIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (80425-0557-3)