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
71335-0321-2	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)
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)
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)
68788-9074-3	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	30 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9074-3)
68788-9074-6	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	60 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9074-6)
68788-9074-8	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	120 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9074-8)
63187-434-30	63187-434	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20150202	N/A	ANDA	ANDA077584	Proficient Rx LP	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-434-30)
70518-3518-2	70518-3518	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20250131	N/A	ANDA	ANDA077584	REMEDYREPACK INC.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	100 POUCH in 1 BOX (70518-3518-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-3518-3)
70518-3518-4	70518-3518	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20250618	N/A	ANDA	ANDA077584	REMEDYREPACK INC.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3518-4)
70518-3518-6	70518-3518	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20260416	N/A	ANDA	ANDA077584	REMEDYREPACK INC.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	45 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3518-6)
61919-513-90	61919-513	HUMAN PRESCRIPTION DRUG	PAROXETINE	PAROXETINE	TABLET, FILM COATED	ORAL	20160229	N/A	ANDA	ANDA077584	DIRECT RX	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (61919-513-90)
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)
63629-1840-3	63629-1840	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20100304	N/A	ANDA	ANDA077584	Bryant Ranch Prepack	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (63629-1840-3)
63629-1840-4	63629-1840	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20100323	N/A	ANDA	ANDA077584	Bryant Ranch Prepack	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63629-1840-4)