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
50090-6023-1	50090-6023	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20220627	N/A	ANDA	ANDA090432	A-S Medication Solutions	ESCITALOPRAM OXALATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-6023-1)
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)
50090-6496-0	50090-6496	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20230524	N/A	ANDA	ANDA090432	A-S Medication Solutions	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-6496-0)
50090-6496-1	50090-6496	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20230526	N/A	ANDA	ANDA090432	A-S Medication Solutions	ESCITALOPRAM OXALATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-6496-1)
70518-1103-0	70518-1103	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20180409	N/A	ANDA	ANDA090432	REMEDYREPACK INC.	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1103-0)