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
71335-1307-8	71335-1307	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20230126	N/A	ANDA	ANDA078032	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	20 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71335-1307-8)
71335-1307-2	71335-1307	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20240403	N/A	ANDA	ANDA078032	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	20 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (71335-1307-2)
71335-1307-3	71335-1307	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20190822	N/A	ANDA	ANDA078032	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1307-3)
71335-1307-4	71335-1307	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20190920	N/A	ANDA	ANDA078032	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1307-4)
51655-277-26	51655-277	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20221005	N/A	ANDA	ANDA078032	Northwind Pharmaceuticals, LLC	ESCITALOPRAM OXALATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-277-26)
51655-277-52	51655-277	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20220908	N/A	ANDA	ANDA078032	Northwind Pharmaceuticals, LLC	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-277-52)
51655-284-26	51655-284	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20200513	N/A	ANDA	ANDA078032	Northwind Pharmaceuticals, LLC	ESCITALOPRAM OXALATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-284-26)
51655-284-52	51655-284	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20220720	N/A	ANDA	ANDA078032	Northwind Pharmaceuticals, LLC	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-284-52)
67296-1408-3	67296-1408	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20210101	N/A	ANDA	ANDA078032	RedPharm Drug, Inc.	ESCITALOPRAM OXALATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67296-1408-3)
72189-424-30	72189-424	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20230208	N/A	ANDA	ANDA078032	Direct_Rx	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72189-424-30)
67296-1421-3	67296-1421	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20210201	N/A	ANDA	ANDA078032	RedPharm Drug, Inc.	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67296-1421-3)
50090-5312-0	50090-5312	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20201029	N/A	ANDA	ANDA078032	A-S Medication Solutions	ESCITALOPRAM OXALATE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-5312-0)
50090-5312-1	50090-5312	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20230713	N/A	ANDA	ANDA078032	A-S Medication Solutions	ESCITALOPRAM OXALATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-5312-1)
72189-451-30	72189-451	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20230330	N/A	ANDA	ANDA078032	Direct_Rx	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72189-451-30)
72189-449-30	72189-449	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20230320	N/A	ANDA	ANDA078032	Direct_Rx	ESCITALOPRAM OXALATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72189-449-30)
72189-451-60	72189-451	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20230330	N/A	ANDA	ANDA078032	Direct_Rx	ESCITALOPRAM OXALATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72189-451-60)
53002-2438-6	53002-2438	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20220501	N/A	ANDA	ANDA078032	RPK Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (53002-2438-6)
53002-2438-3	53002-2438	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20220501	N/A	ANDA	ANDA078032	RPK Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (53002-2438-3)
67296-1597-9	67296-1597	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20120315	N/A	ANDA	ANDA078032	RedPharm Drug, Inc.	ESCITALOPRAM OXALATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (67296-1597-9)
53002-2438-0	53002-2438	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20220501	N/A	ANDA	ANDA078032	RPK Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (53002-2438-0)