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
69097-847-15	69097-847	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram	TABLET, FILM COATED	ORAL	20160616	N/A	ANDA	ANDA078604	Cipla USA Inc.	ESCITALOPRAM OXALATE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (69097-847-15)
69097-848-02	69097-848	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram	TABLET, FILM COATED	ORAL	20160616	N/A	ANDA	ANDA078604	Cipla USA Inc.	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (69097-848-02)
69097-848-05	69097-848	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram	TABLET, FILM COATED	ORAL	20160616	N/A	ANDA	ANDA078604	Cipla USA Inc.	ESCITALOPRAM OXALATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (69097-848-05)
69097-848-07	69097-848	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram	TABLET, FILM COATED	ORAL	20160616	N/A	ANDA	ANDA078604	Cipla USA Inc.	ESCITALOPRAM OXALATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69097-848-07)
69097-848-12	69097-848	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram	TABLET, FILM COATED	ORAL	20160616	N/A	ANDA	ANDA078604	Cipla USA Inc.	ESCITALOPRAM OXALATE	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (69097-848-12)
69097-848-15	69097-848	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram	TABLET, FILM COATED	ORAL	20160616	N/A	ANDA	ANDA078604	Cipla USA Inc.	ESCITALOPRAM OXALATE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (69097-848-15)
69097-849-02	69097-849	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram	TABLET, FILM COATED	ORAL	20160616	N/A	ANDA	ANDA078604	Cipla USA Inc.	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (69097-849-02)
69097-849-05	69097-849	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram	TABLET, FILM COATED	ORAL	20160616	N/A	ANDA	ANDA078604	Cipla USA Inc.	ESCITALOPRAM OXALATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (69097-849-05)
69097-849-07	69097-849	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram	TABLET, FILM COATED	ORAL	20160616	N/A	ANDA	ANDA078604	Cipla USA Inc.	ESCITALOPRAM OXALATE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69097-849-07)
69097-849-12	69097-849	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram	TABLET, FILM COATED	ORAL	20160616	N/A	ANDA	ANDA078604	Cipla USA Inc.	ESCITALOPRAM OXALATE	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (69097-849-12)
69097-849-15	69097-849	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram	TABLET, FILM COATED	ORAL	20160616	N/A	ANDA	ANDA078604	Cipla USA Inc.	ESCITALOPRAM OXALATE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (69097-849-15)
69097-847-05	69097-847	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram	TABLET, FILM COATED	ORAL	20160616	N/A	ANDA	ANDA078604	Cipla USA Inc.	ESCITALOPRAM OXALATE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (69097-847-05)
69097-847-07	69097-847	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram	TABLET, FILM COATED	ORAL	20160616	N/A	ANDA	ANDA078604	Cipla USA Inc.	ESCITALOPRAM OXALATE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69097-847-07)
69097-847-12	69097-847	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram	TABLET, FILM COATED	ORAL	20160616	N/A	ANDA	ANDA078604	Cipla USA Inc.	ESCITALOPRAM OXALATE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (69097-847-12)