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
0378-7003-93	0378-7003	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20080324	N/A	ANDA	ANDA078902	Mylan Pharmaceuticals Inc.	PAROXETINE HYDROCHLORIDE	30 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-7003-93)
43353-554-15	43353-554	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20091105	N/A	ANDA	ANDA078902	Aphena Pharma Solutions - Tennessee, LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43353-554-15)
43353-554-30	43353-554	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20190201	N/A	ANDA	ANDA078902	Aphena Pharma Solutions - Tennessee, LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43353-554-30)
43353-554-45	43353-554	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20140807	N/A	ANDA	ANDA078902	Aphena Pharma Solutions - Tennessee, LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	45 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43353-554-45)
55289-037-45	55289-037	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20110801	N/A	ANDA	ANDA078902	PD-Rx Pharmaceuticals, Inc.	PAROXETINE HYDROCHLORIDE	10 mg/1	45 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-037-45)
55289-037-90	55289-037	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20110801	N/A	ANDA	ANDA078902	PD-Rx Pharmaceuticals, Inc.	PAROXETINE HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-037-90)