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
71335-0321-1	71335-0321	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20180212	N/A	ANDA	ANDA077584	Bryant Ranch Prepack	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0321-1)
71335-0321-2	71335-0321	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20211227	N/A	ANDA	ANDA077584	Bryant Ranch Prepack	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0321-2)
71335-0321-3	71335-0321	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20180517	N/A	ANDA	ANDA077584	Bryant Ranch Prepack	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0321-3)
71335-0321-4	71335-0321	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20211227	N/A	ANDA	ANDA077584	Bryant Ranch Prepack	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71335-0321-4)
65841-098-01	65841-098	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Lifesciences Limited	PAROXETINE HYDROCHLORIDE ANHYDROUS	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65841-098-01)
65841-098-05	65841-098	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Lifesciences Limited	PAROXETINE HYDROCHLORIDE ANHYDROUS	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65841-098-05)
65841-098-06	65841-098	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Lifesciences Limited	PAROXETINE HYDROCHLORIDE ANHYDROUS	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65841-098-06)
65841-098-10	65841-098	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Lifesciences Limited	PAROXETINE HYDROCHLORIDE ANHYDROUS	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65841-098-10)
65841-098-16	65841-098	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Lifesciences Limited	PAROXETINE HYDROCHLORIDE ANHYDROUS	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65841-098-16)
65841-097-01	65841-097	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Lifesciences Limited	PAROXETINE HYDROCHLORIDE ANHYDROUS	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65841-097-01)
65841-097-05	65841-097	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Lifesciences Limited	PAROXETINE HYDROCHLORIDE ANHYDROUS	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65841-097-05)
65841-097-06	65841-097	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Lifesciences Limited	PAROXETINE HYDROCHLORIDE ANHYDROUS	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65841-097-06)
65841-097-10	65841-097	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Lifesciences Limited	PAROXETINE HYDROCHLORIDE ANHYDROUS	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65841-097-10)
65841-097-16	65841-097	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Lifesciences Limited	PAROXETINE HYDROCHLORIDE ANHYDROUS	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65841-097-16)
68788-6870-1	68788-6870	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20170111	N/A	ANDA	ANDA077584	Preferred Pharmaceuticals Inc.	PAROXETINE HYDROCHLORIDE	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68788-6870-1)
68788-6870-3	68788-6870	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20170111	N/A	ANDA	ANDA077584	Preferred Pharmaceuticals Inc.	PAROXETINE HYDROCHLORIDE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-6870-3)
68788-6870-6	68788-6870	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20170111	N/A	ANDA	ANDA077584	Preferred Pharmaceuticals Inc.	PAROXETINE HYDROCHLORIDE	40 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-6870-6)
68788-6870-8	68788-6870	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20170111	N/A	ANDA	ANDA077584	Preferred Pharmaceuticals Inc.	PAROXETINE HYDROCHLORIDE	40 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (68788-6870-8)
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)