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
71335-1030-7	71335-1030	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20250129	N/A	ANDA	ANDA202389	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	10 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (71335-1030-7)
71335-1030-8	71335-1030	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20250129	N/A	ANDA	ANDA202389	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	10 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71335-1030-8)
71335-1030-9	71335-1030	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20220621	N/A	ANDA	ANDA202389	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-1030-9)
68071-4985-3	68071-4985	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20190725	N/A	ANDA	ANDA202389	NuCare Pharmaceuticals,Inc.	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-4985-3)
16729-170-01	16729-170	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20130321	N/A	ANDA	ANDA202389	Accord Healthcare Inc.	ESCITALOPRAM OXALATE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16729-170-01)
16729-169-17	16729-169	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20131112	N/A	ANDA	ANDA202389	Accord Healthcare Inc.	ESCITALOPRAM OXALATE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (16729-169-17)
16729-169-01	16729-169	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20130319	N/A	ANDA	ANDA202389	Accord Healthcare Inc.	ESCITALOPRAM OXALATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16729-169-01)