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
71335-3094-6	71335-3094	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20260217	N/A	ANDA	ANDA078777	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	10 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-3094-6)
71335-3094-7	71335-3094	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20260217	N/A	ANDA	ANDA078777	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	10 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (71335-3094-7)
71335-3094-8	71335-3094	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20260217	N/A	ANDA	ANDA078777	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	10 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71335-3094-8)
71335-3094-9	71335-3094	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20260217	N/A	ANDA	ANDA078777	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-3094-9)
71335-3094-3	71335-3094	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20260217	N/A	ANDA	ANDA078777	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-3094-3)
71335-3094-4	71335-3094	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20260217	N/A	ANDA	ANDA078777	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-3094-4)
71335-3094-1	71335-3094	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20260217	N/A	ANDA	ANDA078777	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-3094-1)
16571-755-01	16571-755	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20230610	N/A	ANDA	ANDA078777	Rising Pharma Holdings, Inc.	ESCITALOPRAM OXALATE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16571-755-01)
16571-755-10	16571-755	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20230610	N/A	ANDA	ANDA078777	Rising Pharma Holdings, Inc.	ESCITALOPRAM OXALATE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (16571-755-10)
16571-756-01	16571-756	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20230610	N/A	ANDA	ANDA078777	Rising Pharma Holdings, Inc.	ESCITALOPRAM OXALATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16571-756-01)
16571-756-10	16571-756	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20230610	N/A	ANDA	ANDA078777	Rising Pharma Holdings, Inc.	ESCITALOPRAM OXALATE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (16571-756-10)
16571-757-01	16571-757	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20230610	N/A	ANDA	ANDA078777	Rising Pharma Holdings, Inc.	ESCITALOPRAM OXALATE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16571-757-01)
16571-757-10	16571-757	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20230610	N/A	ANDA	ANDA078777	Rising Pharma Holdings, Inc.	ESCITALOPRAM OXALATE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (16571-757-10)
67046-1465-3	67046-1465	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20250204	N/A	ANDA	ANDA078777	Coupler LLC	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1465-3)
67046-1472-3	67046-1472	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20250204	N/A	ANDA	ANDA078777	Coupler LLC	ESCITALOPRAM OXALATE	5 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1472-3)