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
63629-9500-1	63629-9500	HUMAN PRESCRIPTION DRUG	PAROXETINE	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180914	N/A	ANDA	ANDA209293	Bryant Ranch Prepack	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	37.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9500-1)
63629-9499-1	63629-9499	HUMAN PRESCRIPTION DRUG	PAROXETINE	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180914	N/A	ANDA	ANDA209293	Bryant Ranch Prepack	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	25 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9499-1)
63629-9498-1	63629-9498	HUMAN PRESCRIPTION DRUG	PAROXETINE	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180914	N/A	ANDA	ANDA209293	Bryant Ranch Prepack	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	12.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9498-1)
42858-703-03	42858-703	HUMAN PRESCRIPTION DRUG	PAROXETINE	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180914	N/A	ANDA	ANDA209293	Rhodes Pharmaceuticals L.P.	PAROXETINE HYDROCHLORIDE	12.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42858-703-03)
42858-707-03	42858-707	HUMAN PRESCRIPTION DRUG	PAROXETINE	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180914	N/A	ANDA	ANDA209293	Rhodes Pharmaceuticals L.P.	PAROXETINE HYDROCHLORIDE	37.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42858-707-03)
42858-707-50	42858-707	HUMAN PRESCRIPTION DRUG	PAROXETINE	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180914	N/A	ANDA	ANDA209293	Rhodes Pharmaceuticals L.P.	PAROXETINE HYDROCHLORIDE	37.5 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42858-707-50)
42858-703-50	42858-703	HUMAN PRESCRIPTION DRUG	PAROXETINE	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180914	N/A	ANDA	ANDA209293	Rhodes Pharmaceuticals L.P.	PAROXETINE HYDROCHLORIDE	12.5 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42858-703-50)
42858-705-03	42858-705	HUMAN PRESCRIPTION DRUG	PAROXETINE	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180914	N/A	ANDA	ANDA209293	Rhodes Pharmaceuticals L.P.	PAROXETINE HYDROCHLORIDE	25 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42858-705-03)
42858-705-50	42858-705	HUMAN PRESCRIPTION DRUG	PAROXETINE	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180914	N/A	ANDA	ANDA209293	Rhodes Pharmaceuticals L.P.	PAROXETINE HYDROCHLORIDE	25 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42858-705-50)