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
55289-053-45	55289-053	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20110401	N/A	ANDA	ANDA078902	PD-Rx Pharmaceuticals, Inc.	PAROXETINE HYDROCHLORIDE	40 mg/1	45 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-053-45)
68788-8777-1	68788-8777	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20250101	N/A	ANDA	ANDA078902	Preferred Pharmaceuticals Inc.	PAROXETINE HYDROCHLORIDE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8777-1)
68788-8777-9	68788-8777	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20250101	N/A	ANDA	ANDA078902	Preferred Pharmaceuticals Inc.	PAROXETINE HYDROCHLORIDE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8777-9)
68788-8777-3	68788-8777	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20250101	N/A	ANDA	ANDA078902	Preferred Pharmaceuticals Inc.	PAROXETINE HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8777-3)
68788-8777-6	68788-8777	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20250101	N/A	ANDA	ANDA078902	Preferred Pharmaceuticals Inc.	PAROXETINE HYDROCHLORIDE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8777-6)
68788-8777-8	68788-8777	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20250101	N/A	ANDA	ANDA078902	Preferred Pharmaceuticals Inc.	PAROXETINE HYDROCHLORIDE	20 mg/1	120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8777-8)