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
50090-5312-1	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)
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)
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)
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)
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)
68788-7461-9	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)
68788-7510-1	68788-7510	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20191227	N/A	ANDA	ANDA078032	Preferred Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68788-7510-1)
68788-7510-3	68788-7510	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20191227	N/A	ANDA	ANDA078032	Preferred Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-7510-3)
68788-7510-6	68788-7510	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20191227	N/A	ANDA	ANDA078032	Preferred Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-7510-6)
68788-7510-8	68788-7510	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20191227	N/A	ANDA	ANDA078032	Preferred Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	10 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (68788-7510-8)
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)
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)
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)
68788-7510-9	68788-7510	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitalopram	TABLET, FILM COATED	ORAL	20191227	N/A	ANDA	ANDA078032	Preferred Pharmaceuticals, Inc.	ESCITALOPRAM OXALATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-7510-9)
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)