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
13668-135-05	13668-135	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20120911	N/A	ANDA	ANDA090939	Torrent Pharmaceuticals Limited	ESCITALOPRAM OXALATE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (13668-135-05)
13668-135-10	13668-135	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20120911	N/A	ANDA	ANDA090939	Torrent Pharmaceuticals Limited	ESCITALOPRAM OXALATE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (13668-135-10)
13668-135-30	13668-135	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20120911	N/A	ANDA	ANDA090939	Torrent Pharmaceuticals Limited	ESCITALOPRAM OXALATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (13668-135-30)
13668-135-40	13668-135	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20120911	N/A	ANDA	ANDA090939	Torrent Pharmaceuticals Limited	ESCITALOPRAM OXALATE	5 mg/1	4000 TABLET, FILM COATED in 1 BOTTLE (13668-135-40)