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
53746-021-05	53746-021	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20170517	N/A	ANDA	ANDA205619	Amneal Pharmaceuticals of New York LLC	ESCITALOPRAM OXALATE	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (53746-021-05)
53746-021-10	53746-021	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20170517	N/A	ANDA	ANDA205619	Amneal Pharmaceuticals of New York LLC	ESCITALOPRAM OXALATE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (53746-021-10)
53746-021-30	53746-021	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20170517	N/A	ANDA	ANDA205619	Amneal Pharmaceuticals of New York LLC	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (53746-021-30)
53746-021-90	53746-021	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20170517	N/A	ANDA	ANDA205619	Amneal Pharmaceuticals of New York LLC	ESCITALOPRAM OXALATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (53746-021-90)