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
69117-0026-3	69117-0026	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20211102	N/A	ANDA	ANDA211248	Yiling Pharmaceutical, Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69117-0026-3)
69117-0026-4	69117-0026	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20211102	N/A	ANDA	ANDA211248	Yiling Pharmaceutical, Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69117-0026-4)
69117-0026-5	69117-0026	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20211102	N/A	ANDA	ANDA211248	Yiling Pharmaceutical, Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69117-0026-5)
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)