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
63629-3349-1	63629-3349	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20090904	N/A	ANDA	ANDA077584	Bryant Ranch Prepack	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63629-3349-1)
63629-3349-2	63629-3349	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20100301	N/A	ANDA	ANDA077584	Bryant Ranch Prepack	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63629-3349-2)
63629-3349-3	63629-3349	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20100317	N/A	ANDA	ANDA077584	Bryant Ranch Prepack	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63629-3349-3)
65841-099-01	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	100 TABLET, FILM COATED in 1 BOTTLE (65841-099-01)
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)
68788-9074-1	68788-9074	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Preferred Pharmaceuticals, Inc	PAROXETINE HYDROCHLORIDE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9074-1)
70518-2465-0	70518-2465	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20191214	N/A	ANDA	ANDA077584	REMEDYREPACK INC.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2465-0)
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)
76420-716-01	76420-716	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20240506	N/A	ANDA	ANDA077584	Asclemed USA, Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (76420-716-01)
76420-716-05	76420-716	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20240506	N/A	ANDA	ANDA077584	Asclemed USA, Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (76420-716-05)
76420-716-10	76420-716	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20240506	N/A	ANDA	ANDA077584	Asclemed USA, Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (76420-716-10)
63629-1840-1	63629-1840	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20230301	N/A	ANDA	ANDA077584	Bryant Ranch Prepack	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63629-1840-1)
63629-1840-2	63629-1840	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20081010	N/A	ANDA	ANDA077584	Bryant Ranch Prepack	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63629-1840-2)