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=ANDA077349"
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
56062-517-71 56062-517 HUMAN OTC DRUG ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20060504 N/A ANDA ANDA077349 Publix Super Markets Inc IBUPROFEN 200 mg/1 1 BOTTLE in 1 CARTON (56062-517-71) / 50 TABLET, FILM COATED in 1 BOTTLE
56062-517-78 56062-517 HUMAN OTC DRUG ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20060503 N/A ANDA ANDA077349 Publix Super Markets Inc IBUPROFEN 200 mg/1 1 BOTTLE in 1 CARTON (56062-517-78) / 100 TABLET, FILM COATED in 1 BOTTLE
50269-000-01 50269-000 HUMAN OTC DRUG MOTRIN IB IBUPROFEN TABLET, FILM COATED ORAL 20181210 N/A ANDA ANDA077349 JC World Bell Wholesale Co., Inc. IBUPROFEN 200 mg/1 6 BLISTER PACK in 1 BOX (50269-000-01) / 1 POUCH in 1 BLISTER PACK / 2 TABLET, FILM COATED in 1 POUCH
50269-000-25 50269-000 HUMAN OTC DRUG MOTRIN IB IBUPROFEN TABLET, FILM COATED ORAL 20181210 N/A ANDA ANDA077349 JC World Bell Wholesale Co., Inc. IBUPROFEN 200 mg/1 25 POUCH in 1 BOX (50269-000-25) / 2 TABLET, FILM COATED in 1 POUCH
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