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
71335-1030-4	71335-1030	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20181219	N/A	ANDA	ANDA202389	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1030-4)
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)
71205-325-30	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)
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)
71205-325-90	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)
71205-344-90	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)