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
62175-471-32	62175-471	HUMAN PRESCRIPTION DRUG	Paroxetine Hydrochloride	Paroxetine Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20141031	N/A	ANDA	ANDA204744	Lannett Company, Inc.	PAROXETINE HYDROCHLORIDE	25 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-471-32)
62175-471-41	62175-471	HUMAN PRESCRIPTION DRUG	Paroxetine Hydrochloride	Paroxetine Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20141031	N/A	ANDA	ANDA204744	Lannett Company, Inc.	PAROXETINE HYDROCHLORIDE	25 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-471-41)
62135-427-30	62135-427	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20221205	N/A	ANDA	ANDA204744	Chartwell RX, LLC	PAROXETINE HYDROCHLORIDE	37.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62135-427-30)
62175-470-32	62175-470	HUMAN PRESCRIPTION DRUG	Paroxetine Hydrochloride	Paroxetine Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20141031	N/A	ANDA	ANDA204744	Lannett Company, Inc.	PAROXETINE HYDROCHLORIDE	12.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-470-32)
62175-470-41	62175-470	HUMAN PRESCRIPTION DRUG	Paroxetine Hydrochloride	Paroxetine Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20141031	N/A	ANDA	ANDA204744	Lannett Company, Inc.	PAROXETINE HYDROCHLORIDE	12.5 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-470-41)
62135-426-30	62135-426	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20221205	N/A	ANDA	ANDA204744	Chartwell RX, LLC	PAROXETINE HYDROCHLORIDE	25 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62135-426-30)
63629-8527-1	63629-8527	HUMAN PRESCRIPTION DRUG	Paroxetine Hydrochloride	Paroxetine Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20141031	N/A	ANDA	ANDA204744	Bryant Ranch Prepack	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	25 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-8527-1)
62135-425-30	62135-425	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20221205	N/A	ANDA	ANDA204744	Chartwell RX, LLC	PAROXETINE HYDROCHLORIDE	12.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62135-425-30)
62175-472-32	62175-472	HUMAN PRESCRIPTION DRUG	Paroxetine Hydrochloride	Paroxetine Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20141031	N/A	ANDA	ANDA204744	Lannett Company, Inc.	PAROXETINE HYDROCHLORIDE	37.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-472-32)
62175-472-41	62175-472	HUMAN PRESCRIPTION DRUG	Paroxetine Hydrochloride	Paroxetine Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20141031	N/A	ANDA	ANDA204744	Lannett Company, Inc.	PAROXETINE HYDROCHLORIDE	37.5 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-472-41)