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
60760-590-90	60760-590	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20231024	N/A	ANDA	ANDA090432	ST. MARY'S MEDICAL PARK PHARMACY	ESCITALOPRAM OXALATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-590-90)
65862-373-01	65862-373	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20120911	N/A	ANDA	ANDA090432	Aurobindo Pharma Limited	ESCITALOPRAM OXALATE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-373-01)
65862-373-05	65862-373	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20120911	N/A	ANDA	ANDA090432	Aurobindo Pharma Limited	ESCITALOPRAM OXALATE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-373-05)
65862-373-10	65862-373	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20120911	N/A	ANDA	ANDA090432	Aurobindo Pharma Limited	ESCITALOPRAM OXALATE	5 mg/1	10 BLISTER PACK in 1 CARTON (65862-373-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
65862-373-19	65862-373	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20120911	N/A	ANDA	ANDA090432	Aurobindo Pharma Limited	ESCITALOPRAM OXALATE	5 mg/1	10000 TABLET, FILM COATED in 1 BOTTLE (65862-373-19)
65862-373-30	65862-373	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20120911	N/A	ANDA	ANDA090432	Aurobindo Pharma Limited	ESCITALOPRAM OXALATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-373-30)
65862-373-90	65862-373	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20120911	N/A	ANDA	ANDA090432	Aurobindo Pharma Limited	ESCITALOPRAM OXALATE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-373-90)