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
71205-168-90	71205-168	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20120911	N/A	ANDA	ANDA090432	Proficient Rx LP	ESCITALOPRAM OXALATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-168-90)
71205-193-60	71205-193	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20190101	N/A	ANDA	ANDA090432	Proficient Rx LP	ESCITALOPRAM OXALATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-193-60)
68084-618-01	68084-618	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20121008	N/A	ANDA	ANDA090432	American Health Packaging	ESCITALOPRAM OXALATE	20 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-618-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-618-11)
71205-193-90	71205-193	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20190101	N/A	ANDA	ANDA090432	Proficient Rx LP	ESCITALOPRAM OXALATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-193-90)
71205-193-30	71205-193	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20190101	N/A	ANDA	ANDA090432	Proficient Rx LP	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-193-30)
42708-077-30	42708-077	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20181218	N/A	ANDA	ANDA090432	QPharma, Inc.	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (42708-077-30)
68084-617-01	68084-617	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20121008	N/A	ANDA	ANDA090432	American Health Packaging	ESCITALOPRAM OXALATE	10 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-617-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-617-11)