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
65862-375-39	65862-375	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20120911	N/A	ANDA	ANDA090432	Aurobindo Pharma Limited	ESCITALOPRAM OXALATE	20 mg/1	3000 TABLET, FILM COATED in 1 BOTTLE (65862-375-39)
65862-375-90	65862-375	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20120911	N/A	ANDA	ANDA090432	Aurobindo Pharma Limited	ESCITALOPRAM OXALATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-375-90)
71335-9687-1	71335-9687	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20230622	N/A	ANDA	ANDA090432	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-9687-1)
71335-9687-2	71335-9687	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20230404	N/A	ANDA	ANDA090432	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-9687-2)
71335-9687-3	71335-9687	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20230710	N/A	ANDA	ANDA090432	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-9687-3)
71335-9687-4	71335-9687	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20241101	N/A	ANDA	ANDA090432	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-9687-4)
76420-722-01	76420-722	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20240506	N/A	ANDA	ANDA090432	Asclemed USA, Inc.	ESCITALOPRAM OXALATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (76420-722-01)
76420-722-05	76420-722	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20240506	N/A	ANDA	ANDA090432	Asclemed USA, Inc.	ESCITALOPRAM OXALATE	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (76420-722-05)
76420-722-10	76420-722	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20240506	N/A	ANDA	ANDA090432	Asclemed USA, Inc.	ESCITALOPRAM OXALATE	10 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (76420-722-10)
76420-722-30	76420-722	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20240506	N/A	ANDA	ANDA090432	Asclemed USA, Inc.	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-722-30)
76420-722-60	76420-722	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20240506	N/A	ANDA	ANDA090432	Asclemed USA, Inc.	ESCITALOPRAM OXALATE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (76420-722-60)
76420-722-90	76420-722	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20240506	N/A	ANDA	ANDA090432	Asclemed USA, Inc.	ESCITALOPRAM OXALATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (76420-722-90)