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)
0378-7004-10	0378-7004	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20080324	N/A	ANDA	ANDA078902	Mylan Pharmaceuticals Inc.	PAROXETINE HYDROCHLORIDE	40 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-7004-10)
0378-7004-93	0378-7004	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20080324	N/A	ANDA	ANDA078902	Mylan Pharmaceuticals Inc.	PAROXETINE HYDROCHLORIDE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-7004-93)
0378-7001-93	0378-7001	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20080324	N/A	ANDA	ANDA078902	Mylan Pharmaceuticals Inc.	PAROXETINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-7001-93)
0378-7002-10	0378-7002	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20080324	N/A	ANDA	ANDA078902	Mylan Pharmaceuticals Inc.	PAROXETINE HYDROCHLORIDE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-7002-10)
0378-7002-93	0378-7002	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20080324	N/A	ANDA	ANDA078902	Mylan Pharmaceuticals Inc.	PAROXETINE HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-7002-93)