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
60505-0083-1	60505-0083	HUMAN PRESCRIPTION DRUG	PAROXETINE	paroxetine hydrochloride	TABLET, FILM COATED	ORAL	20030908	N/A	ANDA	ANDA075356	Apotex Corp.	PAROXETINE HYDROCHLORIDE ANHYDROUS	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (60505-0083-1)
60505-0083-2	60505-0083	HUMAN PRESCRIPTION DRUG	PAROXETINE	paroxetine hydrochloride	TABLET, FILM COATED	ORAL	20030908	N/A	ANDA	ANDA075356	Apotex Corp.	PAROXETINE HYDROCHLORIDE ANHYDROUS	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (60505-0083-2)
60505-0083-4	60505-0083	HUMAN PRESCRIPTION DRUG	PAROXETINE	paroxetine hydrochloride	TABLET, FILM COATED	ORAL	20030908	N/A	ANDA	ANDA075356	Apotex Corp.	PAROXETINE HYDROCHLORIDE ANHYDROUS	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (60505-0083-4)
60505-0084-1	60505-0084	HUMAN PRESCRIPTION DRUG	PAROXETINE	paroxetine hydrochloride	TABLET, FILM COATED	ORAL	20030908	N/A	ANDA	ANDA075356	Apotex Corp.	PAROXETINE HYDROCHLORIDE ANHYDROUS	30 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (60505-0084-1)
60505-0084-2	60505-0084	HUMAN PRESCRIPTION DRUG	PAROXETINE	paroxetine hydrochloride	TABLET, FILM COATED	ORAL	20030908	N/A	ANDA	ANDA075356	Apotex Corp.	PAROXETINE HYDROCHLORIDE ANHYDROUS	30 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (60505-0084-2)
60505-0084-4	60505-0084	HUMAN PRESCRIPTION DRUG	PAROXETINE	paroxetine hydrochloride	TABLET, FILM COATED	ORAL	20030908	N/A	ANDA	ANDA075356	Apotex Corp.	PAROXETINE HYDROCHLORIDE ANHYDROUS	30 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (60505-0084-4)
60505-0097-1	60505-0097	HUMAN PRESCRIPTION DRUG	PAROXETINE	paroxetine hydrochloride	TABLET, FILM COATED	ORAL	20030908	N/A	ANDA	ANDA075356	Apotex Corp.	PAROXETINE HYDROCHLORIDE ANHYDROUS	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (60505-0097-1)
60505-0097-2	60505-0097	HUMAN PRESCRIPTION DRUG	PAROXETINE	paroxetine hydrochloride	TABLET, FILM COATED	ORAL	20030908	N/A	ANDA	ANDA075356	Apotex Corp.	PAROXETINE HYDROCHLORIDE ANHYDROUS	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (60505-0097-2)
60505-0097-4	60505-0097	HUMAN PRESCRIPTION DRUG	PAROXETINE	paroxetine hydrochloride	TABLET, FILM COATED	ORAL	20030908	N/A	ANDA	ANDA075356	Apotex Corp.	PAROXETINE HYDROCHLORIDE ANHYDROUS	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (60505-0097-4)
60505-0101-1	60505-0101	HUMAN PRESCRIPTION DRUG	PAROXETINE	paroxetine hydrochloride	TABLET, FILM COATED	ORAL	20030908	N/A	ANDA	ANDA075356	Apotex Corp.	PAROXETINE HYDROCHLORIDE ANHYDROUS	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (60505-0101-1)
60505-0101-2	60505-0101	HUMAN PRESCRIPTION DRUG	PAROXETINE	paroxetine hydrochloride	TABLET, FILM COATED	ORAL	20030908	N/A	ANDA	ANDA075356	Apotex Corp.	PAROXETINE HYDROCHLORIDE ANHYDROUS	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (60505-0101-2)
60505-0101-4	60505-0101	HUMAN PRESCRIPTION DRUG	PAROXETINE	paroxetine hydrochloride	TABLET, FILM COATED	ORAL	20030908	N/A	ANDA	ANDA075356	Apotex Corp.	PAROXETINE HYDROCHLORIDE ANHYDROUS	40 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (60505-0101-4)
55154-7999-0	55154-7999	HUMAN PRESCRIPTION DRUG	PAROXETINE	paroxetine hydrochloride	TABLET, FILM COATED	ORAL	20030908	N/A	ANDA	ANDA075356	Cardinal Health 107, LLC	PAROXETINE HYDROCHLORIDE ANHYDROUS	20 mg/1	1 BLISTER PACK in 1 BAG (55154-7999-0) / 10 TABLET, FILM COATED in 1 BLISTER PACK
70518-0993-1	70518-0993	HUMAN PRESCRIPTION DRUG	PAROXETINE	paroxetine hydrochloride	TABLET, FILM COATED	ORAL	20200908	N/A	ANDA	ANDA075356	REMEDYREPACK INC.	PAROXETINE HYDROCHLORIDE ANHYDROUS	40 mg/1	100 POUCH in 1 BOX (70518-0993-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-0993-2)
70518-1460-1	70518-1460	HUMAN PRESCRIPTION DRUG	PAROXETINE	paroxetine hydrochloride	TABLET, FILM COATED	ORAL	20201109	N/A	ANDA	ANDA075356	REMEDYREPACK INC.	PAROXETINE HYDROCHLORIDE ANHYDROUS	30 mg/1	100 POUCH in 1 BOX (70518-1460-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-1460-2)