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
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)
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)
68382-001-05	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)
68382-001-01	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)
68382-097-01	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	100 TABLET, FILM COATED in 1 BOTTLE (68382-097-01)
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)
68382-098-01	68382-098	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68382-098-01)
68382-098-05	68382-098	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68382-098-05)
68382-098-06	68382-098	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68382-098-06)
68382-098-10	68382-098	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68382-098-10)
68382-098-16	68382-098	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68382-098-16)
68382-099-01	68382-099	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68382-099-01)
68382-099-05	68382-099	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68382-099-05)
68382-099-06	68382-099	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68382-099-06)
68382-099-10	68382-099	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68382-099-10)
68382-099-16	68382-099	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68382-099-16)
68382-097-05	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	500 TABLET, FILM COATED in 1 BOTTLE (68382-097-05)
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)