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=ANDA090796"
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
63187-451-90 63187-451 HUMAN PRESCRIPTION DRUG ibuprofen ibuprofen TABLET ORAL 20190101 N/A ANDA ANDA090796 Proficient Rx LP IBUPROFEN 600 mg/1 90 TABLET in 1 BOTTLE (63187-451-90)
80425-0243-4 80425-0243 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230110 N/A ANDA ANDA090796 Advanced Rx Pharmacy of Tennessee, LLC IBUPROFEN 800 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (80425-0243-4)
68071-5126-3 68071-5126 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191211 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 400 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-5126-3)
68071-5126-9 68071-5126 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191211 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 400 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-5126-9)
68071-5134-6 68071-5134 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191213 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 400 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (68071-5134-6)
68071-5135-0 68071-5135 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191216 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68071-5135-0)
68071-5140-3 68071-5140 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191231 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 3 TABLET, FILM COATED in 1 BOTTLE (68071-5140-3)
68071-5140-6 68071-5140 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200106 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (68071-5140-6)
70518-0005-6 70518-0005 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20230317 N/A ANDA ANDA090796 REMEDYREPACK INC. IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0005-6)
80425-0393-1 80425-0393 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20240523 N/A ANDA ANDA090796 Advanced Rx of Tennessee, LLC IBUPROFEN 800 mg/1 30 TABLET in 1 BOTTLE (80425-0393-1)
80425-0393-2 80425-0393 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20240523 N/A ANDA ANDA090796 Advanced Rx of Tennessee, LLC IBUPROFEN 800 mg/1 60 TABLET in 1 BOTTLE (80425-0393-2)
80425-0393-3 80425-0393 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20240523 N/A ANDA ANDA090796 Advanced Rx of Tennessee, LLC IBUPROFEN 800 mg/1 90 TABLET in 1 BOTTLE (80425-0393-3)
80425-0393-4 80425-0393 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20240523 N/A ANDA ANDA090796 Advanced Rx of Tennessee, LLC IBUPROFEN 800 mg/1 100 TABLET in 1 BOTTLE (80425-0393-4)
80425-0393-5 80425-0393 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20240523 N/A ANDA ANDA090796 Advanced Rx of Tennessee, LLC IBUPROFEN 800 mg/1 120 TABLET in 1 BOTTLE (80425-0393-5)
80425-0426-1 80425-0426 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20240806 N/A ANDA ANDA090796 Advanced Rx of Tennessee, LLC IBUPROFEN 600 mg/1 30 TABLET in 1 BOTTLE (80425-0426-1)
80425-0426-2 80425-0426 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20240806 N/A ANDA ANDA090796 Advanced Rx of Tennessee, LLC IBUPROFEN 600 mg/1 60 TABLET in 1 BOTTLE (80425-0426-2)
80425-0426-3 80425-0426 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20240806 N/A ANDA ANDA090796 Advanced Rx of Tennessee, LLC IBUPROFEN 600 mg/1 90 TABLET in 1 BOTTLE (80425-0426-3)
80425-0426-4 80425-0426 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20240806 N/A ANDA ANDA090796 Advanced Rx of Tennessee, LLC IBUPROFEN 600 mg/1 100 TABLET in 1 BOTTLE (80425-0426-4)
72189-231-21 72189-231 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20210604 N/A ANDA ANDA090796 DIRECT RX IBUPROFEN 600 mg/1 21 TABLET, FILM COATED in 1 BOTTLE (72189-231-21)
72189-231-30 72189-231 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20210604 N/A ANDA ANDA090796 DIRECT RX IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72189-231-30)
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