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
70518-0003-0	70518-0003	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20161123	N/A	ANDA	ANDA077584	REMEDYREPACK INC.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0003-0)
70518-0003-1	70518-0003	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20220601	N/A	ANDA	ANDA077584	REMEDYREPACK INC.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0003-1)
70518-0003-2	70518-0003	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20240501	N/A	ANDA	ANDA077584	REMEDYREPACK INC.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	30 POUCH in 1 BOX (70518-0003-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-0003-3)
68788-7410-9	68788-7410	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20180606	N/A	ANDA	ANDA077584	Preferred Pharmaceuticals Inc.	PAROXETINE HYDROCHLORIDE	30 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-7410-9)
72189-492-30	72189-492	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20230621	N/A	ANDA	ANDA077584	Direct_Rx	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72189-492-30)