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
62207-729-42 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)
62207-729-49 62207-729 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 (62207-729-49)
51316-761-20 51316-761 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20240525 N/A ANDA ANDA091353 CVS NAPROXEN SODIUM 220 mg/1 200 TABLET in 1 BOTTLE (51316-761-20)
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)
62207-761-42 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 50 TABLET, FILM COATED in 1 BOTTLE (62207-761-42)
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)
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)
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)
62207-762-42 62207-762 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20110930 N/A ANDA ANDA091353 Granules India Ltd NAPROXEN SODIUM 220 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (62207-762-42)
62207-762-43 62207-762 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 (62207-762-43)
62207-762-47 62207-762 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 (62207-762-47)
62207-762-49 62207-762 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 (62207-762-49)
11673-764-05 11673-764 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20240301 N/A ANDA ANDA091353 TARGET CORPORATION NAPROXEN SODIUM 220 mg/1 50 TABLET in 1 BOTTLE (11673-764-05)
11673-764-09 11673-764 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20240301 N/A ANDA ANDA091353 TARGET CORPORATION NAPROXEN SODIUM 220 mg/1 90 TABLET in 1 BOTTLE (11673-764-09)
55758-048-02 55758-048 HUMAN OTC DRUG Rapidol Naproxen Naproxen sodium TABLET, COATED ORAL 20231024 N/A ANDA ANDA091353 Pharmadel LLC NAPROXEN SODIUM 220 mg/1 2 TABLET, COATED in 1 PACKET (55758-048-02)
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)
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)
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