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
71335-1396-1 71335-1396 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191118 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 800 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-1396-1)
71335-1396-2 71335-1396 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191118 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 800 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71335-1396-2)
71335-1396-3 71335-1396 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191118 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 800 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (71335-1396-3)
71335-1396-4 71335-1396 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191118 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 800 mg/1 21 TABLET, FILM COATED in 1 BOTTLE (71335-1396-4)
71335-1396-5 71335-1396 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191118 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1396-5)
71335-1396-6 71335-1396 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191118 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-1396-6)
71335-1396-7 71335-1396 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191118 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 800 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-1396-7)
71335-1396-8 71335-1396 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191118 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 800 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-1396-8)
71335-1396-9 71335-1396 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191118 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 800 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-1396-9)
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)
71335-1503-0 71335-1503 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 600 mg/1 21 TABLET, FILM COATED in 1 BOTTLE (71335-1503-0)
71335-1503-1 71335-1503 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 600 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-1503-1)
71335-1503-2 71335-1503 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 600 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71335-1503-2)
71335-1503-3 71335-1503 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1503-3)
71335-1503-4 71335-1503 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 600 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (71335-1503-4)
71335-1503-5 71335-1503 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 600 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-1503-5)
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