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"
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
41163-707-71 41163-707 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 (41163-707-71) / 50 TABLET, FILM COATED in 1 BOTTLE
41163-707-75 41163-707 HUMAN OTC DRUG equaline naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20211221 N/A ANDA ANDA074661 United Natural Foods, Inc. dba UNFI NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (41163-707-75) / 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)
36800-368-62 36800-368 HUMAN OTC DRUG TopCare All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 19970722 N/A ANDA ANDA074661 Topco Associates LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (36800-368-62) / 24 TABLET, FILM COATED in 1 BOTTLE
36800-368-82 36800-368 HUMAN OTC DRUG TopCare All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20040127 N/A ANDA ANDA074661 Topco Associates LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (36800-368-82) / 200 TABLET, FILM COATED in 1 BOTTLE
36800-368-71 36800-368 HUMAN OTC DRUG TopCare All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 19970114 N/A ANDA ANDA074661 Topco Associates LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (36800-368-71) / 50 TABLET, FILM COATED in 1 BOTTLE
36800-368-75 36800-368 HUMAN OTC DRUG TopCare All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20220712 N/A ANDA ANDA074661 Topco Associates LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (36800-368-75) / 90 TABLET, FILM COATED in 1 BOTTLE
36800-368-76 36800-368 HUMAN OTC DRUG TopCare All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20070629 N/A ANDA ANDA074661 Topco Associates LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (36800-368-76) / 120 TABLET, FILM COATED in 1 BOTTLE
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
0536-1094-11 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
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
0363-0368-71 0363-0368 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 19970114 N/A ANDA ANDA074661 Walgreen Company NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0363-0368-71) / 50 TABLET, FILM COATED in 1 BOTTLE
0363-0368-75 0363-0368 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20220726 N/A ANDA ANDA074661 Walgreen Company NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0363-0368-75) / 90 TABLET, FILM COATED in 1 BOTTLE
0363-0368-76 0363-0368 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20020711 N/A ANDA ANDA074661 Walgreen Company NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0363-0368-76) / 120 TABLET, FILM COATED in 1 BOTTLE
21130-593-79 21130-593 HUMAN OTC DRUG NAPROXEN SODIUM Naproxen Sodium TABLET, FILM COATED ORAL 20250813 N/A ANDA ANDA074661 Safeway NAPROXEN SODIUM 220 mg/1 400 TABLET, FILM COATED in 1 BOTTLE (21130-593-79)
36800-490-62 36800-490 HUMAN OTC DRUG Topcare All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 19970722 N/A ANDA ANDA074661 Topco Associates LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (36800-490-62) / 24 TABLET, FILM COATED in 1 BOTTLE
41250-313-82 41250-313 HUMAN OTC DRUG naproxen sodium Naproxen sodium TABLET, FILM COATED ORAL 20040528 N/A ANDA ANDA074661 Meijer Distribution Inc NAPROXEN SODIUM 220 mg/1 200 TABLET, FILM COATED in 1 BOTTLE (41250-313-82)
36800-490-71 36800-490 HUMAN OTC DRUG Topcare All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 19970114 N/A ANDA ANDA074661 Topco Associates LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (36800-490-71) / 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
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase