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
16714-181-01	16714-181	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	NorthStar Rx LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (16714-181-01)
16714-181-02	16714-181	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	NorthStar Rx LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (16714-181-02)
16714-181-03	16714-181	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	NorthStar Rx LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16714-181-03)
16714-181-04	16714-181	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	NorthStar Rx LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (16714-181-04)
16714-181-05	16714-181	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	NorthStar Rx LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (16714-181-05)
63187-564-30	63187-564	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20181201	N/A	ANDA	ANDA078406	Proficient Rx LP	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-564-30)
63187-564-60	63187-564	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20181201	N/A	ANDA	ANDA078406	Proficient Rx LP	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63187-564-60)
63187-564-90	63187-564	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20181201	N/A	ANDA	ANDA078406	Proficient Rx LP	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63187-564-90)
13107-154-01	13107-154	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20091203	N/A	ANDA	ANDA078406	Aurolife Pharma LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (13107-154-01)
13107-154-05	13107-154	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20091203	N/A	ANDA	ANDA078406	Aurolife Pharma LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (13107-154-05)
16714-182-01	16714-182	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	NorthStar Rx LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (16714-182-01)
16714-182-02	16714-182	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	NorthStar Rx LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (16714-182-02)
16714-182-03	16714-182	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	NorthStar Rx LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16714-182-03)
16714-182-04	16714-182	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	NorthStar Rx LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (16714-182-04)
50268-640-15	50268-640	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20160311	N/A	ANDA	ANDA078406	AvPAK	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-640-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-640-11)
13107-155-01	13107-155	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20091203	N/A	ANDA	ANDA078406	Aurolife Pharma LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (13107-155-01)
13107-155-05	13107-155	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20091203	N/A	ANDA	ANDA078406	Aurolife Pharma LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (13107-155-05)
13107-155-30	13107-155	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20091203	N/A	ANDA	ANDA078406	Aurolife Pharma LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (13107-155-30)
13107-155-90	13107-155	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20091203	N/A	ANDA	ANDA078406	Aurolife Pharma LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (13107-155-90)
16714-183-01	16714-183	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	NorthStar Rx LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (16714-183-01)