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)
检索条件:" 注册申请号=ANDA203854"
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
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)
72789-420-90 72789-420 HUMAN PRESCRIPTION DRUG Paroxetine paroxetine hydrochloride hemihydrate TABLET, FILM COATED ORAL 20240712 N/A ANDA ANDA203854 PD-Rx Pharmaceuticals, Inc. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-420-90)
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)
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)
63187-927-30 63187-927 HUMAN PRESCRIPTION DRUG Paroxetine paroxetine hydrochloride hemihydrate TABLET, FILM COATED ORAL 20171101 N/A ANDA ANDA203854 Proficient Rx LP PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63187-927-30)
63187-927-60 63187-927 HUMAN PRESCRIPTION DRUG Paroxetine paroxetine hydrochloride hemihydrate TABLET, FILM COATED ORAL 20171101 N/A ANDA ANDA203854 Proficient Rx LP PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63187-927-60)
63187-927-90 63187-927 HUMAN PRESCRIPTION DRUG Paroxetine paroxetine hydrochloride hemihydrate TABLET, FILM COATED ORAL 20171101 N/A ANDA ANDA203854 Proficient Rx LP PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63187-927-90)
43547-349-03 43547-349 HUMAN PRESCRIPTION DRUG Paroxetine paroxetine hydrochloride hemihydrate TABLET, FILM COATED ORAL 20220329 N/A ANDA ANDA203854 Solco Healthcare US, LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (43547-349-03)
43547-349-09 43547-349 HUMAN PRESCRIPTION DRUG Paroxetine paroxetine hydrochloride hemihydrate TABLET, FILM COATED ORAL 20220329 N/A ANDA ANDA203854 Solco Healthcare US, LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (43547-349-09)
43547-349-11 43547-349 HUMAN PRESCRIPTION DRUG Paroxetine paroxetine hydrochloride hemihydrate TABLET, FILM COATED ORAL 20220329 N/A ANDA ANDA203854 Solco Healthcare US, LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (43547-349-11)
43547-349-50 43547-349 HUMAN PRESCRIPTION DRUG Paroxetine paroxetine hydrochloride hemihydrate TABLET, FILM COATED ORAL 20220329 N/A ANDA ANDA203854 Solco Healthcare US, LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (43547-349-50)
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)
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)
68788-8829-3 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)
68788-8829-6 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)
70518-2598-0 70518-2598 HUMAN PRESCRIPTION DRUG Paroxetine paroxetine hydrochloride hemihydrate TABLET, FILM COATED ORAL 20200225 N/A ANDA ANDA203854 REMEDYREPACK INC. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 30 POUCH in 1 BOX (70518-2598-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-2598-1)
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)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase