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=ANDA091239"
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
11673-991-20 11673-991 HUMAN OTC DRUG IBUPROFEN IBUPROFEN TABLET, COATED ORAL 20200204 N/A ANDA ANDA091239 TARGET CORPORATION IBUPROFEN 200 mg/1 200 TABLET, COATED in 1 BOTTLE (11673-991-20)
11673-991-50 11673-991 HUMAN OTC DRUG IBUPROFEN IBUPROFEN TABLET, COATED ORAL 20200204 N/A ANDA ANDA091239 TARGET CORPORATION IBUPROFEN 200 mg/1 500 TABLET, COATED in 1 BOTTLE (11673-991-50)
11673-991-88 11673-991 HUMAN OTC DRUG IBUPROFEN IBUPROFEN TABLET, COATED ORAL 20200204 N/A ANDA ANDA091239 TARGET CORPORATION IBUPROFEN 200 mg/1 1000 TABLET, COATED in 1 BOTTLE (11673-991-88)
21130-006-01 21130-006 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET ORAL 20230622 N/A ANDA ANDA091239 BETTER LIVING BRANDS, LLC IBUPROFEN 200 mg/1 1 BOTTLE in 1 CARTON (21130-006-01) / 100 TABLET in 1 BOTTLE
21130-006-05 21130-006 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET ORAL 20230909 N/A ANDA ANDA091239 BETTER LIVING BRANDS, LLC IBUPROFEN 200 mg/1 1 BOTTLE in 1 CARTON (21130-006-05) / 50 TABLET in 1 BOTTLE
21130-006-42 21130-006 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET ORAL 20230622 N/A ANDA ANDA091239 BETTER LIVING BRANDS, LLC IBUPROFEN 200 mg/1 1 BOTTLE in 1 CARTON (21130-006-42) / 24 TABLET in 1 BOTTLE
21130-006-53 21130-006 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET ORAL 20230828 N/A ANDA ANDA091239 BETTER LIVING BRANDS, LLC IBUPROFEN 200 mg/1 500 TABLET in 1 BOTTLE (21130-006-53)
25000-114-02 25000-114 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET ORAL 20191220 N/A ANDA ANDA091239 MARKSANS PHARMA LIMITED IBUPROFEN 200 mg/1 1 BOTTLE in 1 CARTON (25000-114-02) / 24 TABLET in 1 BOTTLE
25000-114-03 25000-114 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET ORAL 20110725 N/A ANDA ANDA091239 MARKSANS PHARMA LIMITED IBUPROFEN 200 mg/1 30 TABLET in 1 BOTTLE (25000-114-03)
25000-114-14 25000-114 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET ORAL 20110725 N/A ANDA ANDA091239 MARKSANS PHARMA LIMITED IBUPROFEN 200 mg/1 1000 TABLET in 1 BOTTLE (25000-114-14)
25000-114-20 25000-114 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET ORAL 20110725 N/A ANDA ANDA091239 MARKSANS PHARMA LIMITED IBUPROFEN 200 mg/1 4 BAG in 1 BOX (25000-114-20) / 6500 TABLET in 1 BAG
25000-114-30 25000-114 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET ORAL 20110725 N/A ANDA ANDA091239 MARKSANS PHARMA LIMITED IBUPROFEN 200 mg/1 6 BAG in 1 BOX (25000-114-30) / 6500 TABLET in 1 BAG
25000-114-70 25000-114 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET ORAL 20110725 N/A ANDA ANDA091239 MARKSANS PHARMA LIMITED IBUPROFEN 200 mg/1 500 TABLET in 1 BOTTLE (25000-114-70)
25000-114-71 25000-114 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET ORAL 20110725 N/A ANDA ANDA091239 MARKSANS PHARMA LIMITED IBUPROFEN 200 mg/1 1000 TABLET in 1 BOTTLE (25000-114-71)
25000-114-93 25000-114 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET ORAL 20110725 N/A ANDA ANDA091239 MARKSANS PHARMA LIMITED IBUPROFEN 200 mg/1 1 BAG in 1 BOX (25000-114-93) / 37470 TABLET in 1 BAG
25000-114-98 25000-114 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET ORAL 20110725 N/A ANDA ANDA091239 MARKSANS PHARMA LIMITED IBUPROFEN 200 mg/1 1 BAG in 1 BOX (25000-114-98) / 34065 TABLET in 1 BAG
25000-117-02 25000-117 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET ORAL 20191220 N/A ANDA ANDA091239 MARKSANS PHARMA LIMITED IBUPROFEN 200 mg/1 1 BOTTLE in 1 CARTON (25000-117-02) / 24 TABLET in 1 BOTTLE
25000-117-03 25000-117 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET ORAL 20110725 N/A ANDA ANDA091239 MARKSANS PHARMA LIMITED IBUPROFEN 200 mg/1 30 TABLET in 1 BOTTLE (25000-117-03)
25000-117-14 25000-117 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET ORAL 20110725 N/A ANDA ANDA091239 MARKSANS PHARMA LIMITED IBUPROFEN 200 mg/1 1000 TABLET in 1 BOTTLE (25000-117-14)
25000-117-20 25000-117 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET ORAL 20110725 N/A ANDA ANDA091239 MARKSANS PHARMA LIMITED IBUPROFEN 200 mg/1 4 BAG in 1 BOX (25000-117-20) / 6500 TABLET in 1 BAG
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase