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
71335-2058-3	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	20220304	N/A	ANDA	ANDA202389	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-2058-4)
50090-4363-0	50090-4363	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20190617	N/A	ANDA	ANDA202389	A-S Medication Solutions	ESCITALOPRAM OXALATE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-4363-0)
51655-149-26	51655-149	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA202389	Northwind Pharmaceuticals	ESCITALOPRAM OXALATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-149-26)
51655-149-52	51655-149	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20210507	N/A	ANDA	ANDA202389	Northwind Pharmaceuticals	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-149-52)
50090-4915-0	50090-4915	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20200218	N/A	ANDA	ANDA202389	A-S Medication Solutions	ESCITALOPRAM OXALATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-4915-0)
51655-236-52	51655-236	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20210510	N/A	ANDA	ANDA202389	Northwind Pharmaceuticals	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-236-52)
51655-449-52	51655-449	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20201020	N/A	ANDA	ANDA202389	Northwind Pharmaceuticals, LLC	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-449-52)
51655-766-52	51655-766	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20210727	N/A	ANDA	ANDA202389	Northwind Pharmaceuticals	ESCITALOPRAM OXALATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-766-52)
53002-1431-0	53002-1431	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20221231	N/A	ANDA	ANDA202389	RPK Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (53002-1431-0)
53002-1431-3	53002-1431	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20221231	N/A	ANDA	ANDA202389	RPK Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (53002-1431-3)
53002-1431-6	53002-1431	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20221231	N/A	ANDA	ANDA202389	RPK Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (53002-1431-6)
72789-194-30	72789-194	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20210622	N/A	ANDA	ANDA202389	PD-Rx Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-194-30)
72789-194-90	72789-194	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20210614	N/A	ANDA	ANDA202389	PD-Rx Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-194-90)