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
72657-111-01	72657-111	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET, FILM COATED	ORAL	20220113	N/A	ANDA	ANDA077654	Glenmark Therapeutics Inc., USA	CITALOPRAM HYDROBROMIDE	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72657-111-01)
72657-111-05	72657-111	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET, FILM COATED	ORAL	20220113	N/A	ANDA	ANDA077654	Glenmark Therapeutics Inc., USA	CITALOPRAM HYDROBROMIDE	40 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72657-111-05)
72657-110-01	72657-110	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET, FILM COATED	ORAL	20220113	N/A	ANDA	ANDA077654	Glenmark Therapeutics Inc., USA	CITALOPRAM HYDROBROMIDE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72657-110-01)
72657-110-05	72657-110	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET, FILM COATED	ORAL	20220113	N/A	ANDA	ANDA077654	Glenmark Therapeutics Inc., USA	CITALOPRAM HYDROBROMIDE	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72657-110-05)
72657-109-01	72657-109	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET, FILM COATED	ORAL	20220113	N/A	ANDA	ANDA077654	Glenmark Therapeutics Inc., USA	CITALOPRAM HYDROBROMIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72657-109-01)
72657-109-05	72657-109	HUMAN PRESCRIPTION DRUG	Citalopram Hydrobromide	Citalopram Hydrobromide	TABLET, FILM COATED	ORAL	20220113	N/A	ANDA	ANDA077654	Glenmark Therapeutics Inc., USA	CITALOPRAM HYDROBROMIDE	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72657-109-05)