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
62135-541-90	62135-541	HUMAN PRESCRIPTION DRUG	PAROXETINE	PAROXETINE	TABLET, FILM COATED	ORAL	20230411	N/A	ANDA	ANDA211248	Chartwell RX, LLC.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (62135-541-90)
62135-542-90	62135-542	HUMAN PRESCRIPTION DRUG	PAROXETINE	PAROXETINE	TABLET, FILM COATED	ORAL	20230411	N/A	ANDA	ANDA211248	Chartwell RX, LLC.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (62135-542-90)
62135-543-90	62135-543	HUMAN PRESCRIPTION DRUG	PAROXETINE	PAROXETINE	TABLET, FILM COATED	ORAL	20230411	N/A	ANDA	ANDA211248	Chartwell RX, LLC.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (62135-543-90)
62135-544-90	62135-544	HUMAN PRESCRIPTION DRUG	PAROXETINE	PAROXETINE	TABLET, FILM COATED	ORAL	20230411	N/A	ANDA	ANDA211248	Chartwell RX, LLC.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (62135-544-90)