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
13668-137-30	13668-137	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20120911	N/A	ANDA	ANDA090939	Torrent Pharmaceuticals Limited	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (13668-137-30)
82009-035-10	82009-035	HUMAN PRESCRIPTION DRUG	escitalopram oxalate	escitalopram oxalate	TABLET	ORAL	20230301	N/A	ANDA	ANDA090939	Quallent Pharmaceuticals Health LLC	ESCITALOPRAM OXALATE	5 mg/1	1000 TABLET in 1 BOTTLE (82009-035-10)
71335-2903-1	71335-2903	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20251022	N/A	ANDA	ANDA090939	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (71335-2903-1)
82982-065-60	82982-065	HUMAN PRESCRIPTION DRUG	escitalopram oxalate	escitalopram oxalate	TABLET	ORAL	20230501	20260731	ANDA	ANDA090939	Pharmasource Meds, LLC	ESCITALOPRAM OXALATE	10 mg/1	60 TABLET in 1 BOTTLE (82982-065-60)