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
51655-277-26	51655-277	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20221005	N/A	ANDA	ANDA078032	Northwind Health Company, LLC	ESCITALOPRAM OXALATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-277-26)
51655-277-52	51655-277	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20220908	N/A	ANDA	ANDA078032	Northwind Health Company, 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 Health Company, LLC	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 Health Company, LLC	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-284-52)
55700-818-30	55700-818	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20191114	20260717	ANDA	ANDA078032	Quality Care Products, LLC	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (55700-818-30)
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)
51655-116-52	51655-116	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20220711	N/A	ANDA	ANDA078032	Northwind Health Company, LLC	ESCITALOPRAM OXALATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-116-52)
71335-1187-1	71335-1187	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20190520	N/A	ANDA	ANDA078032	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1187-1)
71335-1187-2	71335-1187	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20240403	N/A	ANDA	ANDA078032	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	10 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (71335-1187-2)
71335-1187-3	71335-1187	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20190411	N/A	ANDA	ANDA078032	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-1187-3)
71335-1187-4	71335-1187	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20190515	N/A	ANDA	ANDA078032	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1187-4)
71335-1187-5	71335-1187	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20240403	N/A	ANDA	ANDA078032	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	10 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71335-1187-5)
71335-1187-6	71335-1187	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20240403	N/A	ANDA	ANDA078032	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	10 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-1187-6)
71335-1187-7	71335-1187	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20240403	N/A	ANDA	ANDA078032	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	10 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (71335-1187-7)
71335-1187-8	71335-1187	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20240403	N/A	ANDA	ANDA078032	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	10 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71335-1187-8)
71335-1187-9	71335-1187	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20220216	N/A	ANDA	ANDA078032	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-1187-9)
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)
72189-451-30	72189-451	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20230330	N/A	ANDA	ANDA078032	Direct_Rx	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72189-451-30)
72189-451-60	72189-451	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20230330	N/A	ANDA	ANDA078032	Direct_Rx	ESCITALOPRAM OXALATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72189-451-60)
72189-451-90	72189-451	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20230330	N/A	ANDA	ANDA078032	Direct_Rx	ESCITALOPRAM OXALATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72189-451-90)