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=ANDA208499"
符合检索条件的记录共 17 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
0113-8264-60 0113-8264 HUMAN OTC DRUG good sense naproxen sodium diphenhydramine hydrochloride, naproxen sodium TABLET, FILM COATED ORAL 20181228 N/A ANDA ANDA208499 L. Perrigo Company DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM 25 mg/1; 220 mg/1 1 BOTTLE in 1 CARTON (0113-8264-60) / 20 TABLET, FILM COATED in 1 BOTTLE
0113-8264-71 0113-8264 HUMAN OTC DRUG good sense naproxen sodium diphenhydramine hydrochloride, naproxen sodium TABLET, FILM COATED ORAL 20220314 N/A ANDA ANDA208499 L. Perrigo Company DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM 25 mg/1; 220 mg/1 1 BOTTLE in 1 CARTON (0113-8264-71) / 50 TABLET, FILM COATED in 1 BOTTLE
11673-687-27 11673-687 HUMAN OTC DRUG up and up naproxen sodium pm diphenhydramine hydrochloride, naproxen sodium TABLET, FILM COATED ORAL 20220125 N/A ANDA ANDA208499 Target Corporation DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM 25 mg/1; 220 mg/1 1 BOTTLE in 1 CARTON (11673-687-27) / 80 TABLET, FILM COATED in 1 BOTTLE
72288-310-06 72288-310 HUMAN OTC DRUG basic care naproxen sodium pm diphenhydramine hydrochloride, naproxen sodium TABLET, FILM COATED ORAL 20210810 N/A ANDA ANDA208499 Amazon.com Services LLC DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM 25 mg/1; 220 mg/1 1 BOTTLE in 1 CARTON (72288-310-06) / 160 TABLET, FILM COATED in 1 BOTTLE
41163-593-71 41163-593 HUMAN OTC DRUG equaline naproxen sodium pm diphenhydramine hydrochloride, naproxen sodium TABLET, FILM COATED ORAL 20220325 N/A ANDA ANDA208499 United Natural Foods, Inc. dba UNFI DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM 25 mg/1; 220 mg/1 1 BOTTLE in 1 CARTON (41163-593-71) / 50 TABLET, FILM COATED in 1 BOTTLE
21130-639-71 21130-639 HUMAN OTC DRUG NAPROXEN SODIUM PM diphenhydramine hydrochloride, naproxen sodium TABLET, FILM COATED ORAL 20250313 N/A ANDA ANDA208499 Safeway DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM 25 mg/1; 220 mg/1 1 BOTTLE in 1 CARTON (21130-639-71) / 50 TABLET, FILM COATED in 1 BOTTLE
37808-264-27 37808-264 HUMAN OTC DRUG naproxen sodium pm diphenhydramine hydrochloride, naproxen sodium TABLET, FILM COATED ORAL 20201013 N/A ANDA ANDA208499 H E B DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM 25 mg/1; 220 mg/1 1 BOTTLE in 1 CARTON (37808-264-27) / 80 TABLET, FILM COATED in 1 BOTTLE
37808-264-60 37808-264 HUMAN OTC DRUG naproxen sodium pm diphenhydramine hydrochloride, naproxen sodium TABLET, FILM COATED ORAL 20201013 N/A ANDA ANDA208499 H E B DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM 25 mg/1; 220 mg/1 1 BOTTLE in 1 CARTON (37808-264-60) / 20 TABLET, FILM COATED in 1 BOTTLE
30142-383-60 30142-383 HUMAN OTC DRUG naproxen sodium pm diphenhydramine hydrochloride, naproxen sodium TABLET, FILM COATED ORAL 20190620 N/A ANDA ANDA208499 Kroger Company DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM 25 mg/1; 220 mg/1 1 BOTTLE in 1 CARTON (30142-383-60) / 20 TABLET, FILM COATED in 1 BOTTLE
30142-753-27 30142-753 HUMAN OTC DRUG naproxen sodium pm diphenhydramine hydrochloride, naproxen sodium TABLET ORAL 20190620 N/A ANDA ANDA208499 Kroger Company DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM 25 mg/1; 220 mg/1 80 TABLET in 1 BOTTLE (30142-753-27)
41520-264-27 41520-264 HUMAN OTC DRUG careone naproxen sodium pm diphenhydramine hydrochloride, naproxen sodium TABLET, FILM COATED ORAL 20200225 N/A ANDA ANDA208499 American Sales Company DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM 25 mg/1; 220 mg/1 1 BOTTLE in 1 CARTON (41520-264-27) / 80 TABLET, FILM COATED in 1 BOTTLE
41520-264-60 41520-264 HUMAN OTC DRUG careone naproxen sodium pm diphenhydramine hydrochloride, naproxen sodium TABLET, FILM COATED ORAL 20200225 N/A ANDA ANDA208499 American Sales Company DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM 25 mg/1; 220 mg/1 1 BOTTLE in 1 CARTON (41520-264-60) / 20 TABLET, FILM COATED in 1 BOTTLE
55910-858-27 55910-858 HUMAN OTC DRUG dg health naproxen sodium pm diphenhydramine hydrochloride, naproxen sodium TABLET, FILM COATED ORAL 20200710 N/A ANDA ANDA208499 Dolgencorp Inc DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM 25 mg/1; 220 mg/1 1 BOTTLE in 1 CARTON (55910-858-27) / 80 TABLET, FILM COATED in 1 BOTTLE
41250-526-27 41250-526 HUMAN OTC DRUG naproxen sodium pm diphenhydramine hydrochloride, naproxen sodium TABLET, FILM COATED ORAL 20200121 N/A ANDA ANDA208499 Meijer Distribution Inc DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM 25 mg/1; 220 mg/1 1 BOTTLE in 1 CARTON (41250-526-27) / 80 TABLET, FILM COATED in 1 BOTTLE
41250-526-60 41250-526 HUMAN OTC DRUG naproxen sodium pm diphenhydramine hydrochloride, naproxen sodium TABLET, FILM COATED ORAL 20200114 N/A ANDA ANDA208499 Meijer Distribution Inc DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM 25 mg/1; 220 mg/1 1 BOTTLE in 1 CARTON (41250-526-60) / 20 TABLET, FILM COATED in 1 BOTTLE
36800-264-27 36800-264 HUMAN OTC DRUG topcare all night pain relief pm diphenhydramine hydrochloride, naproxen sodium TABLET, FILM COATED ORAL 20190812 N/A ANDA ANDA208499 Topco Associates LLC DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM 25 mg/1; 220 mg/1 1 BOTTLE in 1 CARTON (36800-264-27) / 80 TABLET, FILM COATED in 1 BOTTLE
36800-264-60 36800-264 HUMAN OTC DRUG topcare all night pain relief pm diphenhydramine hydrochloride, naproxen sodium TABLET, FILM COATED ORAL 20190808 N/A ANDA ANDA208499 Topco Associates LLC DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM 25 mg/1; 220 mg/1 1 BOTTLE in 1 CARTON (36800-264-60) / 20 TABLET, FILM COATED in 1 BOTTLE
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