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
43602-474-10	43602-474	HUMAN PRESCRIPTION DRUG	ESCITALOPRAM OXALATE	escitalopram	TABLET	ORAL	20250715	N/A	ANDA	ANDA215177	Ascent Pharmaceuticals, Inc	ESCITALOPRAM OXALATE	10 mg/1	1000 TABLET in 1 BOTTLE (43602-474-10)
43602-474-30	43602-474	HUMAN PRESCRIPTION DRUG	ESCITALOPRAM OXALATE	escitalopram	TABLET	ORAL	20250715	N/A	ANDA	ANDA215177	Ascent Pharmaceuticals, Inc	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET in 1 BOTTLE (43602-474-30)
43602-475-10	43602-475	HUMAN PRESCRIPTION DRUG	ESCITALOPRAM OXALATE	escitalopram	TABLET	ORAL	20250715	N/A	ANDA	ANDA215177	Ascent Pharmaceuticals, Inc	ESCITALOPRAM OXALATE	20 mg/1	1000 TABLET in 1 BOTTLE (43602-475-10)
43602-475-30	43602-475	HUMAN PRESCRIPTION DRUG	ESCITALOPRAM OXALATE	escitalopram	TABLET	ORAL	20250715	N/A	ANDA	ANDA215177	Ascent Pharmaceuticals, Inc	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET in 1 BOTTLE (43602-475-30)
43602-473-10	43602-473	HUMAN PRESCRIPTION DRUG	ESCITALOPRAM OXALATE	escitalopram	TABLET	ORAL	20250715	N/A	ANDA	ANDA215177	Ascent Pharmaceuticals, Inc	ESCITALOPRAM OXALATE	5 mg/1	1000 TABLET in 1 BOTTLE (43602-473-10)
43602-473-30	43602-473	HUMAN PRESCRIPTION DRUG	ESCITALOPRAM OXALATE	escitalopram	TABLET	ORAL	20250715	N/A	ANDA	ANDA215177	Ascent Pharmaceuticals, Inc	ESCITALOPRAM OXALATE	5 mg/1	30 TABLET in 1 BOTTLE (43602-473-30)