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
70518-3518-0	70518-3518	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20220913	N/A	ANDA	ANDA077584	REMEDYREPACK INC.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3518-0)
70518-3518-1	70518-3518	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20220929	N/A	ANDA	ANDA077584	REMEDYREPACK INC.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3518-1)
70518-3518-2	70518-3518	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20250131	N/A	ANDA	ANDA077584	REMEDYREPACK INC.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	100 POUCH in 1 BOX (70518-3518-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-3518-3)
70518-3518-4	70518-3518	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20250618	N/A	ANDA	ANDA077584	REMEDYREPACK INC.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3518-4)
68382-099-01	68382-099	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68382-099-01)
68382-099-05	68382-099	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68382-099-05)
68382-099-06	68382-099	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68382-099-06)
68382-099-10	68382-099	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68382-099-10)
68382-099-16	68382-099	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68382-099-16)
60760-398-90	60760-398	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20190320	N/A	ANDA	ANDA077584	St. Mary's Medical Park Pharmacy	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-398-90)
68382-097-01	68382-097	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68382-097-01)
68382-097-05	68382-097	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68382-097-05)
68382-097-06	68382-097	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68382-097-06)
68382-097-10	68382-097	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68382-097-10)
68382-097-16	68382-097	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20070413	N/A	ANDA	ANDA077584	Zydus Pharmaceuticals USA Inc.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68382-097-16)
68084-045-01	68084-045	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20050315	N/A	ANDA	ANDA077584	American Health Packaging	PAROXETINE HYDROCHLORIDE	20 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-045-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-045-11)
63739-888-10	63739-888	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20150909	20251231	ANDA	ANDA077584	McKesson Corporation dba SKY Packaging	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	10 mg/1	10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-888-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
63187-105-30	63187-105	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20150202	N/A	ANDA	ANDA077584	Proficient Rx LP	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-105-30)
68084-047-01	68084-047	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20050315	N/A	ANDA	ANDA077584	American Health Packaging	PAROXETINE HYDROCHLORIDE	40 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-047-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-047-11)
70518-2465-0	70518-2465	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED	ORAL	20191214	N/A	ANDA	ANDA077584	REMEDYREPACK INC.	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	30 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2465-0)