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
65841-099-05	65841-099	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Lifesciences Limited	PAROXETINE HYDROCHLORIDE ANHYDROUS	30 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65841-099-05)
65841-099-06	65841-099	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Lifesciences Limited	PAROXETINE HYDROCHLORIDE ANHYDROUS	30 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65841-099-06)
65841-099-10	65841-099	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Lifesciences Limited	PAROXETINE HYDROCHLORIDE ANHYDROUS	30 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65841-099-10)
65841-099-16	65841-099	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Lifesciences Limited	PAROXETINE HYDROCHLORIDE ANHYDROUS	30 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65841-099-16)
65841-601-01	65841-601	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Lifesciences Limited	PAROXETINE HYDROCHLORIDE ANHYDROUS	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65841-601-01)
65841-601-05	65841-601	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Lifesciences Limited	PAROXETINE HYDROCHLORIDE ANHYDROUS	40 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65841-601-05)
65841-601-06	65841-601	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Lifesciences Limited	PAROXETINE HYDROCHLORIDE ANHYDROUS	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65841-601-06)
65841-601-10	65841-601	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Lifesciences Limited	PAROXETINE HYDROCHLORIDE ANHYDROUS	40 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65841-601-10)
65841-601-16	65841-601	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Lifesciences Limited	PAROXETINE HYDROCHLORIDE ANHYDROUS	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65841-601-16)
68071-1740-1	68071-1740	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20170818	N/A	ANDA	ANDA077584	NuCare Pharmaceuticals,Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-1740-1)
68788-7410-1	68788-7410	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20180606	N/A	ANDA	ANDA077584	Preferred Pharmaceuticals Inc.	PAROXETINE HYDROCHLORIDE	30 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68788-7410-1)
68788-7410-2	68788-7410	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20180606	N/A	ANDA	ANDA077584	Preferred Pharmaceuticals Inc.	PAROXETINE HYDROCHLORIDE	30 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (68788-7410-2)
68788-7410-3	68788-7410	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20180606	N/A	ANDA	ANDA077584	Preferred Pharmaceuticals Inc.	PAROXETINE HYDROCHLORIDE	30 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-7410-3)
68788-7410-6	68788-7410	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20180606	N/A	ANDA	ANDA077584	Preferred Pharmaceuticals Inc.	PAROXETINE HYDROCHLORIDE	30 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-7410-6)
68788-7410-8	68788-7410	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20180606	N/A	ANDA	ANDA077584	Preferred Pharmaceuticals Inc.	PAROXETINE HYDROCHLORIDE	30 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (68788-7410-8)
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)
68071-2535-9	68071-2535	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20260202	N/A	ANDA	ANDA077584	NuCare Pharamceuticals, Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-2535-9)
55289-972-30	55289-972	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20160210	N/A	ANDA	ANDA077584	PD-Rx Pharmaceuticals, Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-972-30)
55289-972-60	55289-972	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20160210	N/A	ANDA	ANDA077584	PD-Rx Pharmaceuticals, Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-972-60)
55289-972-90	55289-972	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20160210	N/A	ANDA	ANDA077584	PD-Rx Pharmaceuticals, Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-972-90)