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
68788-8829-6	68788-8829	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20250213	N/A	ANDA	ANDA203854	Preferred Pharmaceuticals Inc.	PAROXETINE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-8829-6)
68788-8829-8	68788-8829	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20250213	N/A	ANDA	ANDA203854	Preferred Pharmaceuticals Inc.	PAROXETINE HYDROCHLORIDE	10 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (68788-8829-8)
68788-8829-9	68788-8829	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20250213	N/A	ANDA	ANDA203854	Preferred Pharmaceuticals Inc.	PAROXETINE HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-8829-9)
0615-8174-39	0615-8174	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20180305	N/A	ANDA	ANDA203854	NCS HealthCare of KY, LLC dba Vangard Labs	PAROXETINE HYDROCHLORIDE	40 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8174-39)