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
71335-0321-3	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)
76420-719-01	76420-719	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20240506	N/A	ANDA	ANDA077584	Asclemed USA, Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (76420-719-01)
76420-719-05	76420-719	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20240506	N/A	ANDA	ANDA077584	Asclemed USA, Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (76420-719-05)
76420-719-10	76420-719	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20240506	N/A	ANDA	ANDA077584	Asclemed USA, Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (76420-719-10)
76420-719-30	76420-719	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20240506	N/A	ANDA	ANDA077584	Asclemed USA, Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-719-30)
76420-719-60	76420-719	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20240506	N/A	ANDA	ANDA077584	Asclemed USA, Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (76420-719-60)
76420-719-90	76420-719	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20240506	N/A	ANDA	ANDA077584	Asclemed USA, Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (76420-719-90)
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)
63187-190-30	63187-190	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20150202	N/A	ANDA	ANDA077584	Proficient Rx LP	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-190-30)
63187-190-60	63187-190	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20150202	N/A	ANDA	ANDA077584	Proficient Rx LP	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63187-190-60)
63187-190-90	63187-190	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20150202	N/A	ANDA	ANDA077584	Proficient Rx LP	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63187-190-90)
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)
68382-097-06	68382-097	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68382-097-06)
68382-097-10	68382-097	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68382-097-10)
68382-097-16	68382-097	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68382-097-16)