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=ANDA074661"
符合检索条件的记录共 132 条，共 7 页，当前第 4 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
0536-1093-06 0536-1093 HUMAN OTC DRUG Rugby All Day Relief Naproxen Sodium TABLET, FILM COATED ORAL 20150915 N/A ANDA ANDA074661 Rugby Laboratories NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0536-1093-06) / 50 TABLET, FILM COATED in 1 BOTTLE
0536-1093-11 0536-1093 HUMAN OTC DRUG Rugby All Day Relief Naproxen Sodium TABLET, FILM COATED ORAL 20220318 N/A ANDA ANDA074661 Rugby Laboratories NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0536-1093-11) / 90 TABLET, FILM COATED in 1 BOTTLE
0536-1094-06 0536-1094 HUMAN OTC DRUG rugby all day relief Naproxen Sodium TABLET, FILM COATED ORAL 20150902 N/A ANDA ANDA074661 Rugby Laboratories NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0536-1094-06) / 50 TABLET, FILM COATED in 1 BOTTLE
0536-1094-11 0536-1094 HUMAN OTC DRUG rugby all day relief Naproxen Sodium TABLET, FILM COATED ORAL 20220427 N/A ANDA ANDA074661 Rugby Laboratories NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0536-1094-11) / 90 TABLET, FILM COATED in 1 BOTTLE
11673-368-71 11673-368 HUMAN OTC DRUG up and up naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20090714 N/A ANDA ANDA074661 Target Corporation NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (11673-368-71) / 50 TABLET, FILM COATED in 1 BOTTLE
11673-909-75 11673-909 HUMAN OTC DRUG up and up naproxen sodium naproxen sodium TABLET, FILM COATED ORAL 20220210 N/A ANDA ANDA074661 Target Corporation NAPROXEN SODIUM 220 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (11673-909-75)
36800-140-82 36800-140 HUMAN OTC DRUG Topcare All Day Pain Relief Naproxen sodium TABLET, FILM COATED ORAL 20071203 N/A ANDA ANDA074661 Topco Associates LLC NAPROXEN SODIUM 220 mg/1 200 TABLET, FILM COATED in 1 BOTTLE (36800-140-82)
37808-631-82 37808-631 HUMAN OTC DRUG naproxen sodium Naproxen sodium TABLET, FILM COATED ORAL 20171114 N/A ANDA ANDA074661 H E B NAPROXEN SODIUM 220 mg/1 200 TABLET, FILM COATED in 1 BOTTLE (37808-631-82)
37808-652-62 37808-652 HUMAN OTC DRUG naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20171114 N/A ANDA ANDA074661 H E B NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (37808-652-62) / 24 TABLET, FILM COATED in 1 BOTTLE
37808-652-71 37808-652 HUMAN OTC DRUG naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20171114 N/A ANDA ANDA074661 H E B NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (37808-652-71) / 50 TABLET, FILM COATED in 1 BOTTLE
37808-713-79 37808-713 HUMAN OTC DRUG naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20171003 N/A ANDA ANDA074661 H E B NAPROXEN SODIUM 220 mg/1 400 TABLET, FILM COATED in 1 BOTTLE (37808-713-79)
41163-511-62 41163-511 HUMAN OTC DRUG equaline naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20140924 N/A ANDA ANDA074661 United Natural Foods, Inc. dba UNFI NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (41163-511-62) / 24 TABLET, FILM COATED in 1 BOTTLE
41163-511-71 41163-511 HUMAN OTC DRUG equaline naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20140924 N/A ANDA ANDA074661 United Natural Foods, Inc. dba UNFI NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (41163-511-71) / 50 TABLET, FILM COATED in 1 BOTTLE
41163-511-75 41163-511 HUMAN OTC DRUG equaline naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20220921 N/A ANDA ANDA074661 United Natural Foods, Inc. dba UNFI NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (41163-511-75) / 90 TABLET, FILM COATED in 1 BOTTLE
43063-909-20 43063-909 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20210327 N/A ANDA ANDA074661 PD-Rx Pharmaceuticals, Inc. NAPROXEN SODIUM 220 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-909-20)
43063-909-30 43063-909 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20210327 N/A ANDA ANDA074661 PD-Rx Pharmaceuticals, Inc. NAPROXEN SODIUM 220 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-909-30)
50090-0685-1 50090-0685 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20181031 N/A ANDA ANDA074661 A-S Medication Solutions NAPROXEN SODIUM 220 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (50090-0685-1)
50090-3356-0 50090-3356 HUMAN OTC DRUG rugby all day relief Naproxen Sodium TABLET, FILM COATED ORAL 20180131 N/A ANDA ANDA074661 A-S Medication Solutions NAPROXEN SODIUM 220 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-3356-0)
50090-3356-1 50090-3356 HUMAN OTC DRUG rugby all day relief Naproxen Sodium TABLET, FILM COATED ORAL 20250313 N/A ANDA ANDA074661 A-S Medication Solutions NAPROXEN SODIUM 220 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (50090-3356-1)
55301-368-71 55301-368 HUMAN OTC DRUG exchange select naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20080826 N/A ANDA ANDA074661 Army & Air Force Exchange Service NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (55301-368-71) / 50 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
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase