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
72603-151-01	72603-151	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20240108	N/A	ANDA	ANDA202210	NorthStar RxLLC	ESCITALOPRAM OXALATE	20 mg/21	1000 TABLET, FILM COATED in 1 BOTTLE (72603-151-01)
50090-7200-1	50090-7200	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20240730	N/A	ANDA	ANDA202210	A-S Medication Solutions	ESCITALOPRAM OXALATE	20 mg/21	90 TABLET, FILM COATED in 1 BOTTLE (50090-7200-1)
50090-7200-0	50090-7200	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20240730	N/A	ANDA	ANDA202210	A-S Medication Solutions	ESCITALOPRAM OXALATE	20 mg/21	30 TABLET, FILM COATED in 1 BOTTLE (50090-7200-0)
72603-150-01	72603-150	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20240108	N/A	ANDA	ANDA202210	NorthStar RxLLC	ESCITALOPRAM OXALATE	10 mg/21	1000 TABLET, FILM COATED in 1 BOTTLE (72603-150-01)
72603-149-01	72603-149	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20240108	N/A	ANDA	ANDA202210	NorthStar RxLLC	ESCITALOPRAM OXALATE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (72603-149-01)
50090-7201-0	50090-7201	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20240730	N/A	ANDA	ANDA202210	A-S Medication Solutions	ESCITALOPRAM OXALATE	20 mg/21	90 TABLET, FILM COATED in 1 BOTTLE (50090-7201-0)
33342-037-11	33342-037	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20120911	N/A	ANDA	ANDA202210	Macleods Pharmaceuticals Limited	ESCITALOPRAM OXALATE	10 mg/21	100 TABLET, FILM COATED in 1 BOTTLE (33342-037-11)
33342-037-12	33342-037	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20120911	N/A	ANDA	ANDA202210	Macleods Pharmaceuticals Limited	ESCITALOPRAM OXALATE	10 mg/21	100 TABLET, FILM COATED in 1 CARTON (33342-037-12)
33342-037-15	33342-037	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20150909	N/A	ANDA	ANDA202210	Macleods Pharmaceuticals Limited	ESCITALOPRAM OXALATE	10 mg/21	500 TABLET, FILM COATED in 1 BOTTLE (33342-037-15)
33342-038-11	33342-038	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20120911	N/A	ANDA	ANDA202210	Macleods Pharmaceuticals Limited	ESCITALOPRAM OXALATE	20 mg/21	100 TABLET, FILM COATED in 1 BOTTLE (33342-038-11)
33342-038-12	33342-038	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20120911	N/A	ANDA	ANDA202210	Macleods Pharmaceuticals Limited	ESCITALOPRAM OXALATE	20 mg/21	100 TABLET, FILM COATED in 1 CARTON (33342-038-12)
33342-036-11	33342-036	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20120911	N/A	ANDA	ANDA202210	Macleods Pharmaceuticals Limited	ESCITALOPRAM OXALATE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (33342-036-11)
33342-036-12	33342-036	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20120911	N/A	ANDA	ANDA202210	Macleods Pharmaceuticals Limited	ESCITALOPRAM OXALATE	5 mg/1	100 TABLET, FILM COATED in 1 CARTON (33342-036-12)
33342-036-15	33342-036	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20150909	N/A	ANDA	ANDA202210	Macleods Pharmaceuticals Limited	ESCITALOPRAM OXALATE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (33342-036-15)
33342-038-15	33342-038	HUMAN PRESCRIPTION DRUG	Escitalopram Oxalate	Escitalopram Oxalate	TABLET, FILM COATED	ORAL	20150909	N/A	ANDA	ANDA202210	Macleods Pharmaceuticals Limited	ESCITALOPRAM OXALATE	20 mg/21	500 TABLET, FILM COATED in 1 BOTTLE (33342-038-15)