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
72189-492-30	72189-492	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20230621	N/A	ANDA	ANDA077584	Direct_Rx	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72189-492-30)
80425-0339-1	80425-0339	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20230519	N/A	ANDA	ANDA077584	Advanced Rx Pharmacy of Tennessee, LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (80425-0339-1)
80425-0339-2	80425-0339	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20230519	N/A	ANDA	ANDA077584	Advanced Rx Pharmacy of Tennessee, LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0339-2)
80425-0339-3	80425-0339	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20230519	N/A	ANDA	ANDA077584	Advanced Rx Pharmacy of Tennessee, LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (80425-0339-3)
58118-0183-8	58118-0183	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20170104	N/A	ANDA	ANDA077584	Clinical Solutions Wholesale, LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (58118-0183-8)
49999-632-30	49999-632	HUMAN PRESCRIPTION DRUG	PAROXETINE	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20111108	N/A	ANDA	ANDA077584	Lake Erie Medical DBA Quality Care Products LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (49999-632-30)
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)
68382-001-01	68382-001	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68382-001-01)
68382-001-05	68382-001	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68382-001-05)
68382-001-06	68382-001	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68382-001-06)
68382-001-10	68382-001	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68382-001-10)
68382-001-16	68382-001	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68382-001-16)
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)
68788-0797-1	68788-0797	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Preferred Pharmaceuticals, Inc	PAROXETINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-0797-1)
68788-0797-3	68788-0797	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Preferred Pharmaceuticals, Inc	PAROXETINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-0797-3)
68788-0797-6	68788-0797	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Preferred Pharmaceuticals, Inc	PAROXETINE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-0797-6)