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
43063-761-01	43063-761	HUMAN PRESCRIPTION DRUG	escitalopram oxalate	escitalopram oxalate	TABLET, FILM COATED	ORAL	20170525	N/A	ANDA	ANDA090939	PD-Rx Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-761-01)
43063-761-30	43063-761	HUMAN PRESCRIPTION DRUG	escitalopram oxalate	escitalopram oxalate	TABLET, FILM COATED	ORAL	20170525	N/A	ANDA	ANDA090939	PD-Rx Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-761-30)
43063-761-90	43063-761	HUMAN PRESCRIPTION DRUG	escitalopram oxalate	escitalopram oxalate	TABLET, FILM COATED	ORAL	20170503	N/A	ANDA	ANDA090939	PD-Rx Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-761-90)
0904-6426-61	0904-6426	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20141015	N/A	ANDA	ANDA090939	Major Pharmaceuticals	ESCITALOPRAM OXALATE	10 mg/1	100 BLISTER PACK in 1 CARTON (0904-6426-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK