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
71205-753-60	71205-753	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitslopram	TABLET	ORAL	20230220	N/A	ANDA	ANDA078169	Proficient Rx LP	ESCITALOPRAM OXALATE	20 mg/1	60 TABLET in 1 BOTTLE (71205-753-60)
71205-753-90	71205-753	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitslopram	TABLET	ORAL	20230220	N/A	ANDA	ANDA078169	Proficient Rx LP	ESCITALOPRAM OXALATE	20 mg/1	90 TABLET in 1 BOTTLE (71205-753-90)
70518-2362-0	70518-2362	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitslopram	TABLET	ORAL	20191011	N/A	ANDA	ANDA078169	REMEDYREPACK INC.	ESCITALOPRAM OXALATE	5 mg/1	30 TABLET in 1 BLISTER PACK (70518-2362-0)
50090-5703-0	50090-5703	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitslopram	TABLET	ORAL	20210923	N/A	ANDA	ANDA078169	A-S Medication Solutions	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET in 1 BOTTLE (50090-5703-0)
50090-5703-1	50090-5703	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitslopram	TABLET	ORAL	20210923	N/A	ANDA	ANDA078169	A-S Medication Solutions	ESCITALOPRAM OXALATE	10 mg/1	90 TABLET in 1 BOTTLE (50090-5703-1)
50090-5830-0	50090-5830	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitslopram	TABLET	ORAL	20211026	N/A	ANDA	ANDA078169	A-S Medication Solutions	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET in 1 BOTTLE (50090-5830-0)
50090-5830-1	50090-5830	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitslopram	TABLET	ORAL	20211026	N/A	ANDA	ANDA078169	A-S Medication Solutions	ESCITALOPRAM OXALATE	20 mg/1	90 TABLET in 1 BOTTLE (50090-5830-1)
71205-753-30	71205-753	HUMAN PRESCRIPTION DRUG	Escitalopram	Escitslopram	TABLET	ORAL	20230220	N/A	ANDA	ANDA078169	Proficient Rx LP	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET in 1 BOTTLE (71205-753-30)