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
69986-017-01	69986-017	HUMAN PRESCRIPTION DRUG	paroxetine hydrochloride	paroxetine hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231222	N/A	ANDA	ANDA213612	Sinotherapeutics Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	37.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69986-017-01)
69986-012-01	69986-012	HUMAN PRESCRIPTION DRUG	paroxetine hydrochloride	paroxetine hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231222	N/A	ANDA	ANDA213612	Sinotherapeutics Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	25 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69986-012-01)
69986-012-18	69986-012	HUMAN PRESCRIPTION DRUG	paroxetine hydrochloride	paroxetine hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231222	N/A	ANDA	ANDA213612	Sinotherapeutics Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	25 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 CARTON (69986-012-18)
69986-011-01	69986-011	HUMAN PRESCRIPTION DRUG	paroxetine hydrochloride	paroxetine hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231222	N/A	ANDA	ANDA213612	Sinotherapeutics Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	12.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69986-011-01)
69986-011-18	69986-011	HUMAN PRESCRIPTION DRUG	paroxetine hydrochloride	paroxetine hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231222	N/A	ANDA	ANDA213612	Sinotherapeutics Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	12.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 CARTON (69986-011-18)