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
68071-3843-1	68071-3843	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20250507	N/A	ANDA	ANDA203854	NuCare Pharmaceuticals, Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-3843-1)
72162-2358-9	72162-2358	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20240628	N/A	ANDA	ANDA203854	Bryant Ranch Prepack	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72162-2358-9)
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)
68788-8829-3	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	30 TABLET, FILM COATED in 1 BOTTLE (68788-8829-3)
68788-8829-1	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	100 TABLET, FILM COATED in 1 BOTTLE (68788-8829-1)
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)
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)
0615-7985-05	0615-7985	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20160516	N/A	ANDA	ANDA203854	NCS HealthCare of KY, LLC dba Vangard Labs	PAROXETINE HYDROCHLORIDE	20 mg/1	15 TABLET, FILM COATED in 1 BLISTER PACK (0615-7985-05)
0615-7985-39	0615-7985	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20160516	N/A	ANDA	ANDA203854	NCS HealthCare of KY, LLC dba Vangard Labs	PAROXETINE HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-7985-39)
0615-8173-39	0615-8173	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20180307	N/A	ANDA	ANDA203854	NCS HealthCare of KY, LLC dba Vangard Labs	PAROXETINE HYDROCHLORIDE	30 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8173-39)
70518-1406-0	70518-1406	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20180907	N/A	ANDA	ANDA203854	REMEDYREPACK INC.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1406-0)
70518-1406-1	70518-1406	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20191211	N/A	ANDA	ANDA203854	REMEDYREPACK INC.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	30 POUCH in 1 BOX (70518-1406-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-1406-2)
50090-5987-0	50090-5987	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20220602	N/A	ANDA	ANDA203854	A-S Medication Solutions	PAROXETINE HYDROCHLORIDE ANHYDROUS	30 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-5987-0)
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)
70518-2182-1	70518-2182	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20191023	N/A	ANDA	ANDA203854	REMEDYREPACK INC.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	30 POUCH in 1 BOX, UNIT-DOSE (70518-2182-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-2182-2)
71205-198-30	71205-198	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20190101	N/A	ANDA	ANDA203854	Proficient Rx LP	PAROXETINE HYDROCHLORIDE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-198-30)
71205-198-90	71205-198	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20190101	N/A	ANDA	ANDA203854	Proficient Rx LP	PAROXETINE HYDROCHLORIDE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-198-90)
70518-1253-1	70518-1253	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20220114	N/A	ANDA	ANDA203854	REMEDYREPACK INC.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	40 mg/1	30 POUCH in 1 BOX (70518-1253-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-1253-2)
70518-2387-0	70518-2387	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20191024	N/A	ANDA	ANDA203854	REMEDYREPACK INC.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	30 POUCH in 1 BOX (70518-2387-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-2387-1)
70518-2387-2	70518-2387	HUMAN PRESCRIPTION DRUG	Paroxetine	paroxetine hydrochloride hemihydrate	TABLET, FILM COATED	ORAL	20210805	N/A	ANDA	ANDA203854	REMEDYREPACK INC.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	30 POUCH in 1 BOX (70518-2387-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-2387-3)