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
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)
16729-170-01	16729-170	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20130321	N/A	ANDA	ANDA202389	Accord Healthcare Inc.	ESCITALOPRAM OXALATE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16729-170-01)
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)
16729-170-17	16729-170	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20131112	N/A	ANDA	ANDA202389	Accord Healthcare Inc.	ESCITALOPRAM OXALATE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (16729-170-17)
16729-169-01	16729-169	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20130319	N/A	ANDA	ANDA202389	Accord Healthcare Inc.	ESCITALOPRAM OXALATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16729-169-01)
16729-169-17	16729-169	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20131112	N/A	ANDA	ANDA202389	Accord Healthcare Inc.	ESCITALOPRAM OXALATE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (16729-169-17)