美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=NAPROXEN"
商品名 申请号 产品号 申请类型 活性成分 剂型/给药途径 规格/剂量 RLD RS 申请号原始批准/暂定批准日期 产品号批准日期 申请人 市场状态
NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE 213663 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM TABLET;ORAL 25MG;220MG No No 2020/09/24 2020/09/24 GRANULES Over-the-counter
NAPROXEN 211910 001 ANDA NAPROXEN SUSPENSION;ORAL 25MG/ML No No 2021/03/10 2021/03/10 NOVITIUM PHARMA Prescription
NAPROXEN AND ESOMEPRAZOLE MAGNESIUM 204920 001 ANDA ESOMEPRAZOLE MAGNESIUM; NAPROXEN TABLET, DELAYED RELEASE;ORAL EQ 20MG BASE;375MG No No 2021/07/20 2021/07/20 MYLAN Discontinued
NAPROXEN AND ESOMEPRAZOLE MAGNESIUM 204920 002 ANDA ESOMEPRAZOLE MAGNESIUM; NAPROXEN TABLET, DELAYED RELEASE;ORAL EQ 20MG BASE;500MG No No 2021/07/20 2021/07/20 MYLAN Discontinued
NAPROXEN SODIUM AND PSEUDOEPHEDRINE HYDROCHLORIDE 211360 001 ANDA NAPROXEN SODIUM; PSEUDOEPHEDRINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 220MG;120MG No No 2022/06/01 2022/06/01 AUROBINDO PHARMA Discontinued
NAPROXEN 215776 001 ANDA NAPROXEN SUSPENSION;ORAL 25MG/ML No No 2022/06/07 2022/06/07 HETERO LABS LTD III Prescription
NAPROXEN SODIUM 215472 001 ANDA NAPROXEN SODIUM CAPSULE;ORAL EQ 200MG BASE No No 2022/08/17 2022/08/17 STRIDES PHARMA Discontinued
NAPROXEN AND ESOMEPRAZOLE MAGNESIUM 204470 001 ANDA ESOMEPRAZOLE MAGNESIUM; NAPROXEN TABLET, DELAYED RELEASE;ORAL EQ 20MG BASE;375MG No No 2022/08/24 2022/08/24 ACTAVIS LABS FL INC Discontinued
NAPROXEN AND ESOMEPRAZOLE MAGNESIUM 204470 002 ANDA ESOMEPRAZOLE MAGNESIUM; NAPROXEN TABLET, DELAYED RELEASE;ORAL EQ 20MG BASE;500MG No No 2022/08/24 2022/08/24 ACTAVIS LABS FL INC Discontinued
NAPROXEN AND ESOMEPRAZOLE MAGNESIUM 213699 001 ANDA ESOMEPRAZOLE MAGNESIUM; NAPROXEN TABLET, DELAYED RELEASE;ORAL EQ 20MG BASE;375MG No No 2022/10/06 2022/10/06 AJANTA PHARMA LTD Prescription
NAPROXEN AND ESOMEPRAZOLE MAGNESIUM 213699 002 ANDA ESOMEPRAZOLE MAGNESIUM; NAPROXEN TABLET, DELAYED RELEASE;ORAL EQ 20MG BASE;500MG No No 2022/10/06 2022/10/06 AJANTA PHARMA LTD Prescription
NAPROXEN SODIUM 211065 001 ANDA NAPROXEN SODIUM TABLET;ORAL 220MG No No 2022/10/28 2022/10/28 HETERO LABS LTD V Over-the-counter
NAPROXEN SODIUM 214463 001 ANDA NAPROXEN SODIUM CAPSULE;ORAL EQ 200MG BASE No No 2023/01/10 2023/01/10 PATHEON SOFTGELS Over-the-counter
NAPROXEN 216908 001 ANDA NAPROXEN TABLET, DELAYED RELEASE;ORAL 375MG No No 2023/05/31 2023/05/31 TULEX PHARMS INC Prescription
NAPROXEN 216908 002 ANDA NAPROXEN TABLET, DELAYED RELEASE;ORAL 500MG No No 2023/05/31 2023/05/31 TULEX PHARMS INC Prescription
NAPROXEN AND ESOMEPRAZOLE MAGNESIUM 217738 001 ANDA ESOMEPRAZOLE MAGNESIUM; NAPROXEN TABLET, DELAYED RELEASE;ORAL EQ 20MG BASE;375MG No No 2023/10/11 2023/10/11 SCIEGEN PHARMS INC Prescription
NAPROXEN AND ESOMEPRAZOLE MAGNESIUM 217738 002 ANDA ESOMEPRAZOLE MAGNESIUM; NAPROXEN TABLET, DELAYED RELEASE;ORAL EQ 20MG BASE;500MG No No 2023/10/11 2023/10/11 SCIEGEN PHARMS INC Prescription
药品名称,活性成分,申请号搜索 高级检索
©2006-2024 DrugFuture->U.S. FDA Drugs Database