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
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)
71205-782-90	71205-782	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20230328	N/A	ANDA	ANDA078032	Proficient Rx LP	ESCITALOPRAM OXALATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-782-90)
43547-280-10	43547-280	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20160201	N/A	ANDA	ANDA078032	SOLCO HEALTHCARE US, LLC	ESCITALOPRAM OXALATE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (43547-280-10)
43547-280-11	43547-280	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20160201	N/A	ANDA	ANDA078032	SOLCO HEALTHCARE US, LLC	ESCITALOPRAM OXALATE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (43547-280-11)
71205-782-30	71205-782	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20230328	N/A	ANDA	ANDA078032	Proficient Rx LP	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-782-30)
71205-782-60	71205-782	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20230328	N/A	ANDA	ANDA078032	Proficient Rx LP	ESCITALOPRAM OXALATE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-782-60)
67296-1421-3	67296-1421	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20210201	N/A	ANDA	ANDA078032	RedPharm Drug, Inc.	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67296-1421-3)
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)
43547-282-11	43547-282	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20160201	N/A	ANDA	ANDA078032	SOLCO HEALTHCARE US, LLC	ESCITALOPRAM OXALATE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (43547-282-11)
70518-2317-0	70518-2317	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20190909	N/A	ANDA	ANDA078032	REMEDYREPACK INC.	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2317-0)
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)
70518-2317-3	70518-2317	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20230921	N/A	ANDA	ANDA078032	REMEDYREPACK INC.	ESCITALOPRAM OXALATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2317-3)
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)
70518-2472-0	70518-2472	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20191206	N/A	ANDA	ANDA078032	REMEDYREPACK INC.	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2472-0)
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)
70518-2472-4	70518-2472	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20231129	N/A	ANDA	ANDA078032	REMEDYREPACK INC.	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2472-4)
51655-116-26	51655-116	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20221201	N/A	ANDA	ANDA078032	Northwind Pharmaceuticals, LLC	ESCITALOPRAM OXALATE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-116-26)
51655-116-52	51655-116	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20220711	N/A	ANDA	ANDA078032	Northwind Pharmaceuticals, LLC	ESCITALOPRAM OXALATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-116-52)
43547-282-10	43547-282	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20160201	N/A	ANDA	ANDA078032	SOLCO HEALTHCARE US, LLC	ESCITALOPRAM OXALATE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (43547-282-10)
70934-630-90	70934-630	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20200318	20241130	ANDA	ANDA078032	Denton Pharma, Inc. DBA Northwind Pharmaceuticals	ESCITALOPRAM OXALATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-630-90)