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
62207-750-47 62207-750 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20110930 N/A ANDA ANDA091353 Granules India Limited NAPROXEN SODIUM 220 mg/1 500 TABLET in 1 BOTTLE (62207-750-47)
62207-750-49 62207-750 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20110930 N/A ANDA ANDA091353 Granules India Limited NAPROXEN SODIUM 220 mg/1 1000 TABLET in 1 BOTTLE (62207-750-49)
62207-750-51 62207-750 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20110930 N/A ANDA ANDA091353 Granules India Limited NAPROXEN SODIUM 220 mg/1 10 TABLET in 1 BOTTLE (62207-750-51)
62207-750-52 62207-750 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20110930 N/A ANDA ANDA091353 Granules India Limited NAPROXEN SODIUM 220 mg/1 300 TABLET in 1 BOTTLE (62207-750-52)
62207-750-53 62207-750 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20110930 N/A ANDA ANDA091353 Granules India Limited NAPROXEN SODIUM 220 mg/1 400 TABLET in 1 BOTTLE (62207-750-53)
51316-762-70 51316-762 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20240525 N/A ANDA ANDA091353 CVS NAPROXEN SODIUM 220 mg/1 270 TABLET in 1 BOTTLE (51316-762-70)
59726-256-15 59726-256 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET ORAL 20140328 20241228 ANDA ANDA091353 P & L Development, LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 BOX (59726-256-15) / 15 TABLET in 1 BOTTLE, PLASTIC
62207-761-49 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 1000 TABLET, FILM COATED in 1 BOTTLE (62207-761-49)
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)
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