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
69584-674-90	69584-674	HUMAN PRESCRIPTION DRUG	paroxetine hydrochloride	paroxetine hydrochloride	TABLET, FILM COATED	ORAL	20221114	N/A	ANDA	ANDA076968	Oxford Pharmaceuticals, LLC	PAROXETINE HYDROCHLORIDE	40 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (69584-674-90)
71335-9650-3	71335-9650	HUMAN PRESCRIPTION DRUG	paroxetine hydrochloride	paroxetine hydrochloride	TABLET, FILM COATED	ORAL	20240906	N/A	ANDA	ANDA076968	Bryant Ranch Prepack	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-9650-3)
71335-9650-2	71335-9650	HUMAN PRESCRIPTION DRUG	paroxetine hydrochloride	paroxetine hydrochloride	TABLET, FILM COATED	ORAL	20240906	N/A	ANDA	ANDA076968	Bryant Ranch Prepack	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-9650-2)
71335-9650-1	71335-9650	HUMAN PRESCRIPTION DRUG	paroxetine hydrochloride	paroxetine hydrochloride	TABLET, FILM COATED	ORAL	20230328	N/A	ANDA	ANDA076968	Bryant Ranch Prepack	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-9650-1)