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
50090-5312-0	50090-5312	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20201029	N/A	ANDA	ANDA078032	A-S Medication Solutions	ESCITALOPRAM OXALATE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-5312-0)
50090-5312-1	50090-5312	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20230713	N/A	ANDA	ANDA078032	A-S Medication Solutions	ESCITALOPRAM OXALATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-5312-1)
71335-1307-1	71335-1307	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20200206	N/A	ANDA	ANDA078032	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-1307-1)
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)
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)
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)
51655-116-26	51655-116	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20221201	N/A	ANDA	ANDA078032	Northwind Health Company, 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 Health Company, LLC	ESCITALOPRAM OXALATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-116-52)
50090-6190-0	50090-6190	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20221028	N/A	ANDA	ANDA078032	A-S Medication Solutions	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-6190-0)
50090-6190-1	50090-6190	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20221028	N/A	ANDA	ANDA078032	A-S Medication Solutions	ESCITALOPRAM OXALATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-6190-1)
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)
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)