美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE"
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 209726 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM TABLET;ORAL 25MG;220MG No No 2018/10/23 2018/10/23 AMNEAL PHARMS CO Over-the-counter
NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE 207597 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM TABLET;ORAL 25MG;220MG No No 2019/01/25 2019/01/25 P AND L Discontinued
NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE 208499 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM TABLET;ORAL 25MG;220MG No No 2019/05/10 2019/05/10 PERRIGO R AND D Over-the-counter
NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE 211830 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM TABLET;ORAL 25MG;220MG No No 2019/08/22 2019/08/22 COREPHARMA Over-the-counter
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
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