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
63187-217-90	63187-217	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20141107	N/A	ANDA	ANDA076765	Proficient Rx LP	ESCITALOPRAM OXALATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63187-217-90)
63187-217-60	63187-217	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20141107	N/A	ANDA	ANDA076765	Proficient Rx LP	ESCITALOPRAM OXALATE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63187-217-60)
63187-217-30	63187-217	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20141107	N/A	ANDA	ANDA076765	Proficient Rx LP	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-217-30)
63187-281-60	63187-281	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20141107	N/A	ANDA	ANDA076765	Proficient Rx LP	ESCITALOPRAM OXALATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63187-281-60)
63187-281-30	63187-281	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20141107	N/A	ANDA	ANDA076765	Proficient Rx LP	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-281-30)
63187-281-90	63187-281	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20141107	N/A	ANDA	ANDA076765	Proficient Rx LP	ESCITALOPRAM OXALATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63187-281-90)