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
71335-2331-7	71335-2331	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20241211	N/A	ANDA	ANDA078777	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	20 mg/1	45 TABLET, FILM COATED in 1 BOTTLE (71335-2331-7)
71335-2331-8	71335-2331	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20241211	N/A	ANDA	ANDA078777	Bryant Ranch Prepack	ESCITALOPRAM OXALATE	20 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71335-2331-8)
70518-4239-0	70518-4239	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20241213	N/A	ANDA	ANDA078777	REMEDYREPACK INC.	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4239-0)
70518-4239-1	70518-4239	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20250225	N/A	ANDA	ANDA078777	REMEDYREPACK INC.	ESCITALOPRAM OXALATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4239-1)
70518-4239-2	70518-4239	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20250619	N/A	ANDA	ANDA078777	REMEDYREPACK INC.	ESCITALOPRAM OXALATE	20 mg/1	7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4239-2)
70518-4239-3	70518-4239	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20250701	N/A	ANDA	ANDA078777	REMEDYREPACK INC.	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4239-3)
67046-1472-3	67046-1472	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20250204	N/A	ANDA	ANDA078777	Coupler LLC	ESCITALOPRAM OXALATE	5 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1472-3)