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
71335-9650-4	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	180 TABLET, FILM COATED in 1 BOTTLE (71335-9650-4)
69584-671-10	69584-671	HUMAN PRESCRIPTION DRUG	paroxetine hydrochloride	paroxetine hydrochloride	TABLET, FILM COATED	ORAL	20221114	N/A	ANDA	ANDA076968	Oxford Pharmaceuticals, LLC	PAROXETINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69584-671-10)
69584-671-09	69584-671	HUMAN PRESCRIPTION DRUG	paroxetine hydrochloride	paroxetine hydrochloride	TABLET, FILM COATED	ORAL	20221114	N/A	ANDA	ANDA076968	Oxford Pharmaceuticals, LLC	PAROXETINE HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (69584-671-09)
69584-671-03	69584-671	HUMAN PRESCRIPTION DRUG	paroxetine hydrochloride	paroxetine hydrochloride	TABLET, FILM COATED	ORAL	20221114	N/A	ANDA	ANDA076968	Oxford Pharmaceuticals, LLC	PAROXETINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (69584-671-03)