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
71335-3009-4 71335-3009 HUMAN PRESCRIPTION DRUG Rugby All Day Relief Naproxen Sodium TABLET, FILM COATED ORAL 20260204 N/A ANDA ANDA074661 Bryant Ranch Prepack NAPROXEN SODIUM 220 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (71335-3009-4)
71335-3009-5 71335-3009 HUMAN PRESCRIPTION DRUG Rugby All Day Relief Naproxen Sodium TABLET, FILM COATED ORAL 20260204 N/A ANDA ANDA074661 Bryant Ranch Prepack NAPROXEN SODIUM 220 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-3009-5)
71335-3009-6 71335-3009 HUMAN PRESCRIPTION DRUG Rugby All Day Relief Naproxen Sodium TABLET, FILM COATED ORAL 20260204 N/A ANDA ANDA074661 Bryant Ranch Prepack NAPROXEN SODIUM 220 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (71335-3009-6)
71335-3009-7 71335-3009 HUMAN PRESCRIPTION DRUG Rugby All Day Relief Naproxen Sodium TABLET, FILM COATED ORAL 20260204 N/A ANDA ANDA074661 Bryant Ranch Prepack NAPROXEN SODIUM 220 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-3009-7)
71335-3009-8 71335-3009 HUMAN PRESCRIPTION DRUG Rugby All Day Relief Naproxen Sodium TABLET, FILM COATED ORAL 20260204 N/A ANDA ANDA074661 Bryant Ranch Prepack NAPROXEN SODIUM 220 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-3009-8)
71335-3009-9 71335-3009 HUMAN PRESCRIPTION DRUG Rugby All Day Relief Naproxen Sodium TABLET, FILM COATED ORAL 20260204 N/A ANDA ANDA074661 Bryant Ranch Prepack NAPROXEN SODIUM 220 mg/1 24 TABLET, FILM COATED in 1 BOTTLE (71335-3009-9)
70677-1137-1 70677-1137 HUMAN OTC DRUG foster and thrive all day pain relief Naproxen Sodium TABLET, FILM COATED ORAL 20231023 N/A ANDA ANDA074661 Strategic Sourcing Services LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (70677-1137-1) / 50 TABLET, FILM COATED in 1 BOTTLE
70677-1137-2 70677-1137 HUMAN OTC DRUG foster and thrive all day pain relief Naproxen Sodium TABLET, FILM COATED ORAL 20230914 N/A ANDA ANDA074661 Strategic Sourcing Services LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (70677-1137-2) / 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
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)
71335-1061-1 71335-1061 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20211228 N/A ANDA ANDA074661 Bryant Ranch Prepack NAPROXEN SODIUM 220 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-1061-1)
71335-1061-2 71335-1061 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20190116 N/A ANDA ANDA074661 Bryant Ranch Prepack NAPROXEN SODIUM 220 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1061-2)
71335-1061-3 71335-1061 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20211228 N/A ANDA ANDA074661 Bryant Ranch Prepack NAPROXEN SODIUM 220 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (71335-1061-3)
71335-1061-4 71335-1061 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20211228 N/A ANDA ANDA074661 Bryant Ranch Prepack NAPROXEN SODIUM 220 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (71335-1061-4)
71335-1061-5 71335-1061 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20211228 N/A ANDA ANDA074661 Bryant Ranch Prepack NAPROXEN SODIUM 220 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-1061-5)
71335-1061-6 71335-1061 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20211228 N/A ANDA ANDA074661 Bryant Ranch Prepack NAPROXEN SODIUM 220 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (71335-1061-6)
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