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
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)
55700-818-90	55700-818	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20191114	20260720	ANDA	ANDA078032	Quality Care Products, LLC	ESCITALOPRAM OXALATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (55700-818-90)
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)
70518-2317-1	70518-2317	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20191115	N/A	ANDA	ANDA078032	REMEDYREPACK INC.	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2317-1)
70518-2317-2	70518-2317	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20200811	N/A	ANDA	ANDA078032	REMEDYREPACK INC.	ESCITALOPRAM OXALATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2317-2)
60687-865-01	60687-865	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20250320	N/A	ANDA	ANDA078032	American Health Packaging	ESCITALOPRAM OXALATE	5 mg/1	100 BLISTER PACK in 1 CARTON (60687-865-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-865-11)
43547-281-10	43547-281	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20160201	N/A	ANDA	ANDA078032	SOLCO HEALTHCARE US, LLC	ESCITALOPRAM OXALATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (43547-281-10)
43547-281-11	43547-281	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20160201	N/A	ANDA	ANDA078032	SOLCO HEALTHCARE US, LLC	ESCITALOPRAM OXALATE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (43547-281-11)
68788-7510-1	68788-7510	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20191227	N/A	ANDA	ANDA078032	Preferred Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68788-7510-1)
68788-7510-3	68788-7510	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20191227	N/A	ANDA	ANDA078032	Preferred Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-7510-3)
68788-7510-6	68788-7510	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20191227	N/A	ANDA	ANDA078032	Preferred Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-7510-6)
68788-7510-8	68788-7510	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20191227	N/A	ANDA	ANDA078032	Preferred Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	10 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (68788-7510-8)
68788-7510-9	68788-7510	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20191227	N/A	ANDA	ANDA078032	Preferred Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-7510-9)
55700-847-30	55700-847	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20200306	20260727	ANDA	ANDA078032	Quality Care Products, LLC	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (55700-847-30)
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)