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
65862-154-90	65862-154	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	Aurobindo Pharma Limited	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-154-90)
65862-154-99	65862-154	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	Aurobindo Pharma Limited	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-154-99)
65862-155-01	65862-155	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	Aurobindo Pharma Limited	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-155-01)
65862-155-05	65862-155	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	Aurobindo Pharma Limited	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-155-05)
65862-155-30	65862-155	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	Aurobindo Pharma Limited	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-155-30)
65862-155-90	65862-155	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	Aurobindo Pharma Limited	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-155-90)
65862-155-99	65862-155	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	Aurobindo Pharma Limited	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-155-99)
65862-156-01	65862-156	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	Aurobindo Pharma Limited	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-156-01)
65862-156-05	65862-156	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	Aurobindo Pharma Limited	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-156-05)
65862-156-30	65862-156	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	Aurobindo Pharma Limited	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-156-30)
65862-156-90	65862-156	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	Aurobindo Pharma Limited	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-156-90)
65862-156-99	65862-156	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	Aurobindo Pharma Limited	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-156-99)
65862-157-01	65862-157	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	Aurobindo Pharma Limited	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-157-01)
65862-157-05	65862-157	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	Aurobindo Pharma Limited	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-157-05)
65862-157-30	65862-157	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	Aurobindo Pharma Limited	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-157-30)
65862-157-90	65862-157	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	Aurobindo Pharma Limited	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-157-90)
65862-157-99	65862-157	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine Hydrochloride	TABLET, FILM COATED	ORAL	20070725	N/A	ANDA	ANDA078406	Aurobindo Pharma Limited	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-157-99)
50268-640-15	50268-640	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20160311	N/A	ANDA	ANDA078406	AvPAK	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-640-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-640-11)
50268-642-15	50268-642	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20160311	N/A	ANDA	ANDA078406	AvPAK	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-642-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-642-11)
50268-643-15	50268-643	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20160311	N/A	ANDA	ANDA078406	AvPAK	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-643-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-643-11)