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
68788-7461-1	68788-7461	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20191227	N/A	ANDA	ANDA078032	Preferred Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68788-7461-1)
68788-7461-3	68788-7461	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20191227	N/A	ANDA	ANDA078032	Preferred Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-7461-3)
68788-7461-6	68788-7461	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20191227	N/A	ANDA	ANDA078032	Preferred Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-7461-6)
68788-7461-8	68788-7461	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20191227	N/A	ANDA	ANDA078032	Preferred Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	20 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (68788-7461-8)
68788-7461-9	68788-7461	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20191227	N/A	ANDA	ANDA078032	Preferred Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-7461-9)
51655-277-52	51655-277	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20220908	N/A	ANDA	ANDA078032	Northwind Pharmaceuticals, LLC	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-277-52)
51655-284-26	51655-284	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20200513	N/A	ANDA	ANDA078032	Northwind Pharmaceuticals	ESCITALOPRAM OXALATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-284-26)
51655-284-52	51655-284	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20220720	N/A	ANDA	ANDA078032	Northwind Pharmaceuticals	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-284-52)
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)
80425-0320-1	80425-0320	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20230411	N/A	ANDA	ANDA078032	Advanced Rx Pharmacy of Tennessee, LLC	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (80425-0320-1)
80425-0320-2	80425-0320	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20230411	N/A	ANDA	ANDA078032	Advanced Rx Pharmacy of Tennessee, LLC	ESCITALOPRAM OXALATE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0320-2)
80425-0320-3	80425-0320	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20230411	N/A	ANDA	ANDA078032	Advanced Rx Pharmacy of Tennessee, LLC	ESCITALOPRAM OXALATE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0320-3)