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
42708-163-30	42708-163	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20230313	N/A	ANDA	ANDA078032	QPharma, Inc.	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-163-30)
68001-591-00	68001-591	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20231218	N/A	ANDA	ANDA078032	BluePoint Laboratories	ESCITALOPRAM OXALATE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68001-591-00)
68001-592-00	68001-592	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20231214	N/A	ANDA	ANDA078032	BluePoint Laboratories	ESCITALOPRAM OXALATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68001-592-00)
68001-592-08	68001-592	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20231214	N/A	ANDA	ANDA078032	BluePoint Laboratories	ESCITALOPRAM OXALATE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68001-592-08)
68001-593-00	68001-593	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20231218	N/A	ANDA	ANDA078032	BluePoint Laboratories	ESCITALOPRAM OXALATE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68001-593-00)
68001-593-08	68001-593	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20231213	N/A	ANDA	ANDA078032	BluePoint Laboratories	ESCITALOPRAM OXALATE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68001-593-08)
70518-2317-4	70518-2317	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20260320	N/A	ANDA	ANDA078032	REMEDYREPACK INC.	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2317-4)
70518-2472-1	70518-2472	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20200422	N/A	ANDA	ANDA078032	REMEDYREPACK INC.	ESCITALOPRAM OXALATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2472-1)
70518-2597-2	70518-2597	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20230919	N/A	ANDA	ANDA078032	REMEDYREPACK INC.	ESCITALOPRAM OXALATE	5 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2597-2)
71335-1307-1	71335-1307	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20200206	N/A	ANDA	ANDA078032	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-1307-1)
71335-1307-2	71335-1307	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20240403	N/A	ANDA	ANDA078032	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	20 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (71335-1307-2)
71335-1307-3	71335-1307	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20190822	N/A	ANDA	ANDA078032	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1307-3)
71335-1307-4	71335-1307	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20190920	N/A	ANDA	ANDA078032	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1307-4)
71335-1307-5	71335-1307	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20200629	N/A	ANDA	ANDA078032	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	20 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-1307-5)
71335-1307-6	71335-1307	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20200827	N/A	ANDA	ANDA078032	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-1307-6)
71335-1307-7	71335-1307	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20240403	N/A	ANDA	ANDA078032	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	20 mg/1	45 TABLET, FILM COATED in 1 BOTTLE (71335-1307-7)
71335-1307-8	71335-1307	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20230126	N/A	ANDA	ANDA078032	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	20 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71335-1307-8)
72189-424-30	72189-424	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20230208	N/A	ANDA	ANDA078032	Direct_Rx	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72189-424-30)
72189-424-90	72189-424	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20230208	N/A	ANDA	ANDA078032	Direct_Rx	ESCITALOPRAM OXALATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72189-424-90)
72189-449-30	72189-449	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20230320	N/A	ANDA	ANDA078032	Direct_Rx	ESCITALOPRAM OXALATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72189-449-30)