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=ANDA091353"
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
55758-048-24 55758-048 HUMAN OTC DRUG Rapidol Naproxen Naproxen sodium TABLET, COATED ORAL 20191009 N/A ANDA ANDA091353 Pharmadel LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (55758-048-24) / 24 TABLET, COATED in 1 BOTTLE
55758-048-50 55758-048 HUMAN OTC DRUG Rapidol Naproxen Naproxen sodium TABLET, COATED ORAL 20231024 N/A ANDA ANDA091353 Pharmadel LLC NAPROXEN SODIUM 220 mg/1 25 PACKET in 1 CARTON (55758-048-50) / 2 TABLET, COATED in 1 PACKET (55758-048-02)
69517-109-02 69517-109 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium Tablets, 220 mg TABLET ORAL 20160407 N/A ANDA ANDA091353 HealthLife of USA LLC NAPROXEN SODIUM 220 mg/1 2 POUCH in 1 POUCH (69517-109-02) / 2 TABLET in 1 POUCH
69517-109-04 69517-109 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium Tablets, 220 mg TABLET ORAL 20160407 N/A ANDA ANDA091353 HealthLife of USA LLC NAPROXEN SODIUM 220 mg/1 400 BOTTLE in 1 BOTTLE (69517-109-04) / 100 BOTTLE in 1 BOTTLE (69517-109-01) / 24 CARTON in 1 BOTTLE (69517-109-24) / 1 TABLET in 1 CARTON
69517-109-25 69517-109 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium Tablets, 220 mg TABLET ORAL 20160407 N/A ANDA ANDA091353 HealthLife of USA LLC NAPROXEN SODIUM 220 mg/1 25 POUCH in 1 BOX (69517-109-25) / 2 TABLET in 1 POUCH
69517-109-50 69517-109 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium Tablets, 220 mg TABLET ORAL 20160407 N/A ANDA ANDA091353 HealthLife of USA LLC NAPROXEN SODIUM 220 mg/1 50 POUCH in 1 BOX (69517-109-50) / 2 TABLET in 1 POUCH
62207-728-24 62207-728 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20180608 N/A ANDA ANDA091353 Granules India Ltd NAPROXEN SODIUM 220 mg/1 24 TABLET in 1 BOTTLE (62207-728-24)
62207-728-42 62207-728 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20180608 N/A ANDA ANDA091353 Granules India Ltd NAPROXEN SODIUM 220 mg/1 50 TABLET in 1 BOTTLE (62207-728-42)
21130-062-05 21130-062 HUMAN OTC DRUG Naproxen Naproxen TABLET ORAL 20230830 N/A ANDA ANDA091353 Safeway, Inc NAPROXEN SODIUM 220 mg/1 50 TABLET in 1 BOTTLE (21130-062-05)
21130-062-09 21130-062 HUMAN OTC DRUG Naproxen Naproxen TABLET ORAL 20230830 N/A ANDA ANDA091353 Safeway, Inc NAPROXEN SODIUM 220 mg/1 90 TABLET in 1 BOTTLE (21130-062-09)
21130-062-20 21130-062 HUMAN OTC DRUG Naproxen Naproxen TABLET ORAL 20230930 N/A ANDA ANDA091353 Safeway, Inc NAPROXEN SODIUM 220 mg/1 200 TABLET in 1 BOTTLE (21130-062-20)
62207-728-43 62207-728 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20180608 N/A ANDA ANDA091353 Granules India Ltd NAPROXEN SODIUM 220 mg/1 100 TABLET in 1 BOTTLE (62207-728-43)
62207-728-47 62207-728 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20180608 N/A ANDA ANDA091353 Granules India Ltd NAPROXEN SODIUM 220 mg/1 500 TABLET in 1 BOTTLE (62207-728-47)
21130-061-05 21130-061 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20230930 N/A ANDA ANDA091353 Safeway, Inc NAPROXEN SODIUM 220 mg/1 50 TABLET in 1 BOTTLE (21130-061-05)
21130-061-09 21130-061 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20230930 N/A ANDA ANDA091353 Safeway, Inc NAPROXEN SODIUM 220 mg/1 90 TABLET in 1 BOTTLE (21130-061-09)
62207-728-49 62207-728 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20180608 N/A ANDA ANDA091353 Granules India Ltd NAPROXEN SODIUM 220 mg/1 1000 TABLET in 1 BOTTLE (62207-728-49)
62207-761-43 62207-761 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20110930 N/A ANDA ANDA091353 Granules India Ltd NAPROXEN SODIUM 220 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (62207-761-43)
37835-594-01 37835-594 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20250301 N/A ANDA ANDA091353 Bi-Mart NAPROXEN SODIUM 220 mg/1 100 TABLET in 1 BOTTLE (37835-594-01)
37835-594-03 37835-594 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20250301 N/A ANDA ANDA091353 Bi-Mart NAPROXEN SODIUM 220 mg/1 300 TABLET in 1 BOTTLE (37835-594-03)
62207-761-47 62207-761 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20110930 N/A ANDA ANDA091353 Granules India Ltd NAPROXEN SODIUM 220 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (62207-761-47)
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