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
69729-123-12 69729-123 HUMAN OTC DRUG PROXEN NP 660 Naproxen Sodium TABLET ORAL 20231107 N/A ANDA ANDA091353 OPMX LLC NAPROXEN SODIUM 220 mg/1 1 BLISTER PACK in 1 CARTON (69729-123-12) / 12 TABLET in 1 BLISTER PACK
68210-4096-1 68210-4096 HUMAN OTC DRUG NAPROXEN SODIUM NAPROXEN SODIUM TABLET, FILM COATED, EXTENDED RELEASE ORAL 20200702 N/A ANDA ANDA091353 SPIRIT PHARMACEUTICALS,LLC NAPROXEN SODIUM 220 mg/1 365 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68210-4096-1)
69729-123-50 69729-123 HUMAN OTC DRUG PROXEN NP 660 Naproxen Sodium TABLET ORAL 20231107 N/A ANDA ANDA091353 OPMX LLC NAPROXEN SODIUM 220 mg/1 50 POUCH in 1 CARTON (69729-123-50) / 2 TABLET in 1 POUCH
69729-123-24 69729-123 HUMAN OTC DRUG PROXEN NP 660 Naproxen Sodium TABLET ORAL 20231116 N/A ANDA ANDA091353 OPMX LLC NAPROXEN SODIUM 220 mg/1 2 BLISTER PACK in 1 CARTON (69729-123-24) / 12 TABLET in 1 BLISTER PACK
62207-327-43 62207-327 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20210716 N/A ANDA ANDA091353 Granules India Ltd NAPROXEN SODIUM 220 mg/1 100 TABLET in 1 BOTTLE (62207-327-43)
62207-327-49 62207-327 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20210716 N/A ANDA ANDA091353 Granules India Ltd NAPROXEN SODIUM 220 mg/1 1000 TABLET in 1 BOTTLE (62207-327-49)
62207-328-41 62207-328 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20210716 N/A ANDA ANDA091353 Granules India Ltd NAPROXEN SODIUM 220 mg/1 24 TABLET in 1 BOTTLE (62207-328-41)
62207-328-42 62207-328 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20210716 N/A ANDA ANDA091353 Granules India Ltd NAPROXEN SODIUM 220 mg/1 50 TABLET in 1 BOTTLE (62207-328-42)
62207-328-43 62207-328 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20210716 N/A ANDA ANDA091353 Granules India Ltd NAPROXEN SODIUM 220 mg/1 100 TABLET in 1 BOTTLE (62207-328-43)
62207-328-47 62207-328 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20210716 N/A ANDA ANDA091353 Granules India Ltd NAPROXEN SODIUM 220 mg/1 500 TABLET in 1 BOTTLE (62207-328-47)
62207-328-49 62207-328 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20210716 N/A ANDA ANDA091353 Granules India Ltd NAPROXEN SODIUM 220 mg/1 1000 TABLET in 1 BOTTLE (62207-328-49)
62207-327-47 62207-327 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20210716 N/A ANDA ANDA091353 Granules India Ltd NAPROXEN SODIUM 220 mg/1 500 TABLET in 1 BOTTLE (62207-327-47)
62207-327-41 62207-327 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20210716 N/A ANDA ANDA091353 Granules India Ltd NAPROXEN SODIUM 220 mg/1 24 TABLET in 1 BOTTLE (62207-327-41)
62207-327-42 62207-327 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20210716 N/A ANDA ANDA091353 Granules India Ltd NAPROXEN SODIUM 220 mg/1 50 TABLET in 1 BOTTLE (62207-327-42)
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)
62207-728-49 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)
62207-729-24 62207-729 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 (62207-729-24)
62207-729-42 62207-729 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 (62207-729-42)
62207-729-43 62207-729 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 (62207-729-43)
62207-729-47 62207-729 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 (62207-729-47)
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