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
60505-1317-3	60505-1317	HUMAN PRESCRIPTION DRUG	PAROXETINE HYDROCHLORIDE	paroxetine hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190809	N/A	NDA AUTHORIZED GENERIC	NDA020936	Apotex Corp	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	25 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-1317-3)
60505-4378-3	60505-4378	HUMAN PRESCRIPTION DRUG	PAXIL CR	paroxetine hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20110101	N/A	NDA	NDA020936	Apotex Corp	PAROXETINE HYDROCHLORIDE	25 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-4378-3)
60505-4377-3	60505-4377	HUMAN PRESCRIPTION DRUG	PAXIL CR	paroxetine hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20110101	N/A	NDA	NDA020936	Apotex Corp	PAROXETINE HYDROCHLORIDE	12.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-4377-3)
60505-1318-3	60505-1318	HUMAN PRESCRIPTION DRUG	PAROXETINE HYDROCHLORIDE	paroxetine hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190809	N/A	NDA AUTHORIZED GENERIC	NDA020936	Apotex Corp	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	37.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-1318-3)
60505-4379-3	60505-4379	HUMAN PRESCRIPTION DRUG	PAXIL CR	paroxetine hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20110101	N/A	NDA	NDA020936	Apotex Corp	PAROXETINE HYDROCHLORIDE	37.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-4379-3)
60505-1316-3	60505-1316	HUMAN PRESCRIPTION DRUG	PAROXETINE HYDROCHLORIDE	paroxetine hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190809	N/A	NDA AUTHORIZED GENERIC	NDA020936	Apotex Corp	PAROXETINE HYDROCHLORIDE	12.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-1316-3)