美国FDA药品数据库-药物在线

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