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=ANDA091625"
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
76282-712-46 76282-712 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220310 N/A ANDA ANDA091625 EXELAN PHARMACEUTICALS, INC. IBUPROFEN 400 mg/1 100 BLISTER PACK in 1 CARTON (76282-712-46) / 10 TABLET, FILM COATED in 1 BLISTER PACK (76282-712-45)
76282-712-50 76282-712 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220310 N/A ANDA ANDA091625 EXELAN PHARMACEUTICALS, INC. IBUPROFEN 400 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76282-712-50)
76282-712-55 76282-712 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220310 N/A ANDA ANDA091625 EXELAN PHARMACEUTICALS, INC. IBUPROFEN 400 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (76282-712-55)
76282-713-10 76282-713 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220310 N/A ANDA ANDA091625 EXELAN PHARMACEUTICALS, INC. IBUPROFEN 600 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76282-713-10)
76282-713-50 76282-713 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220310 N/A ANDA ANDA091625 EXELAN PHARMACEUTICALS, INC. IBUPROFEN 600 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76282-713-50)
76282-713-55 76282-713 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220310 N/A ANDA ANDA091625 EXELAN PHARMACEUTICALS, INC. IBUPROFEN 600 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (76282-713-55)
76282-714-10 76282-714 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220310 N/A ANDA ANDA091625 EXELAN PHARMACEUTICALS, INC. IBUPROFEN 800 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76282-714-10)
76282-714-30 76282-714 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220310 N/A ANDA ANDA091625 EXELAN PHARMACEUTICALS, INC. IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76282-714-30)
76282-714-46 76282-714 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220310 N/A ANDA ANDA091625 EXELAN PHARMACEUTICALS, INC. IBUPROFEN 800 mg/1 100 BLISTER PACK in 1 CARTON (76282-714-46) / 10 TABLET, FILM COATED in 1 BLISTER PACK (76282-714-45)
76282-714-50 76282-714 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220310 N/A ANDA ANDA091625 EXELAN PHARMACEUTICALS, INC. IBUPROFEN 800 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76282-714-50)
76282-714-55 76282-714 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220310 N/A ANDA ANDA091625 EXELAN PHARMACEUTICALS, INC. IBUPROFEN 800 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (76282-714-55)
76282-714-90 76282-714 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220310 N/A ANDA ANDA091625 EXELAN PHARMACEUTICALS, INC. IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76282-714-90)
70518-1051-0 70518-1051 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20180301 N/A ANDA ANDA091625 REMEDYREPACK INC. IBUPROFEN 400 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1051-0)
70518-1051-2 70518-1051 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20201211 N/A ANDA ANDA091625 REMEDYREPACK INC. IBUPROFEN 400 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1051-2)
70518-1051-4 70518-1051 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20250721 N/A ANDA ANDA091625 REMEDYREPACK INC. IBUPROFEN 400 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1051-4)
50090-2548-0 50090-2548 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20170213 N/A ANDA ANDA091625 A-S Medication Solutions IBUPROFEN 800 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (50090-2548-0)
50090-2548-1 50090-2548 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20161208 N/A ANDA ANDA091625 A-S Medication Solutions IBUPROFEN 800 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (50090-2548-1)
50090-2548-2 50090-2548 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20161020 N/A ANDA ANDA091625 A-S Medication Solutions IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-2548-2)
50090-2548-3 50090-2548 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20170106 N/A ANDA ANDA091625 A-S Medication Solutions IBUPROFEN 800 mg/1 45 TABLET, FILM COATED in 1 BOTTLE (50090-2548-3)
50090-2548-4 50090-2548 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20161027 N/A ANDA ANDA091625 A-S Medication Solutions IBUPROFEN 800 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-2548-4)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase