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
71205-344-30	71205-344	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20191101	N/A	ANDA	ANDA202389	Proficient Rx LP	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-344-30)
71205-344-60	71205-344	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20191101	N/A	ANDA	ANDA202389	Proficient Rx LP	ESCITALOPRAM OXALATE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-344-60)
71205-344-90	71205-344	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20191101	N/A	ANDA	ANDA202389	Proficient Rx LP	ESCITALOPRAM OXALATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-344-90)
71610-425-60	71610-425	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20200508	N/A	ANDA	ANDA202389	Aphena Pharma Solutions - Tennessee, LLC	ESCITALOPRAM OXALATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71610-425-60)
71205-325-90	71205-325	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20190901	N/A	ANDA	ANDA202389	Proficient Rx LP	ESCITALOPRAM OXALATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-325-90)
71205-325-60	71205-325	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20190901	N/A	ANDA	ANDA202389	Proficient Rx LP	ESCITALOPRAM OXALATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-325-60)
71205-325-30	71205-325	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20190901	N/A	ANDA	ANDA202389	Proficient Rx LP	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-325-30)
71335-2058-1	71335-2058	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20220630	N/A	ANDA	ANDA202389	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2058-1)
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)
68071-3069-3	68071-3069	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20170310	N/A	ANDA	ANDA202389	NuCare Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-3069-3)
68071-3069-8	68071-3069	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20170310	N/A	ANDA	ANDA202389	NuCare Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	20 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (68071-3069-8)
51655-149-26	51655-149	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA202389	Northwind Health Company, LLC	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 Health Company, LLC	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)
71335-2058-2	71335-2058	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20250131	N/A	ANDA	ANDA202389	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-2058-2)
51655-449-52	51655-449	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20201020	N/A	ANDA	ANDA202389	Northwind Health Company, 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 Health Company, LLC	ESCITALOPRAM OXALATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-766-52)
16729-168-01	16729-168	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20130305	N/A	ANDA	ANDA202389	Accord Healthcare Inc.	ESCITALOPRAM OXALATE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16729-168-01)
16729-168-17	16729-168	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20140723	N/A	ANDA	ANDA202389	Accord Healthcare Inc.	ESCITALOPRAM OXALATE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (16729-168-17)