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
71610-425-60	71610-425	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20200508	N/A	ANDA	ANDA202389	Aphena Pharma Solutions - Tennessee, LLC	ESCITALOPRAM OXALATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71610-425-60)
68071-3069-3	68071-3069	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20170310	N/A	ANDA	ANDA202389	NuCare Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-3069-3)
68071-3069-8	68071-3069	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20170310	N/A	ANDA	ANDA202389	NuCare Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	20 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (68071-3069-8)
71335-2058-1	71335-2058	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20220630	N/A	ANDA	ANDA202389	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2058-1)
71335-2058-2	71335-2058	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20250131	N/A	ANDA	ANDA202389	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-2058-2)
71335-2058-3	71335-2058	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20220304	N/A	ANDA	ANDA202389	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-2058-3)
71335-2058-4	71335-2058	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20250131	N/A	ANDA	ANDA202389	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-2058-4)