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=ANDA213794"
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
68788-8354-8 68788-8354 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230210 N/A ANDA ANDA213794 Preferred Pharmaceuticals Inc. IBUPROFEN 600 mg/1 120 TABLET in 1 BOTTLE (68788-8354-8)
68788-8354-9 68788-8354 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230210 N/A ANDA ANDA213794 Preferred Pharmaceuticals Inc. IBUPROFEN 600 mg/1 90 TABLET in 1 BOTTLE (68788-8354-9)
59651-360-01 59651-360 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20200508 N/A ANDA ANDA213794 Aurobindo Pharma Limited IBUPROFEN 400 mg/1 100 TABLET in 1 BOTTLE (59651-360-01)
59651-360-05 59651-360 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20200508 N/A ANDA ANDA213794 Aurobindo Pharma Limited IBUPROFEN 400 mg/1 500 TABLET in 1 BOTTLE (59651-360-05)
68788-8354-2 68788-8354 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230210 N/A ANDA ANDA213794 Preferred Pharmaceuticals Inc. IBUPROFEN 600 mg/1 20 TABLET in 1 BOTTLE (68788-8354-2)
68788-8354-3 68788-8354 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230210 N/A ANDA ANDA213794 Preferred Pharmaceuticals Inc. IBUPROFEN 600 mg/1 30 TABLET in 1 BOTTLE (68788-8354-3)
68788-8354-4 68788-8354 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230210 N/A ANDA ANDA213794 Preferred Pharmaceuticals Inc. IBUPROFEN 600 mg/1 14 TABLET in 1 BOTTLE (68788-8354-4)
68788-8438-1 68788-8438 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230428 N/A ANDA ANDA213794 Preferred Pharmaceuticals Inc. IBUPROFEN 400 mg/1 100 TABLET in 1 BOTTLE (68788-8438-1)
68788-8438-6 68788-8438 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230428 N/A ANDA ANDA213794 Preferred Pharmaceuticals Inc. IBUPROFEN 400 mg/1 60 TABLET in 1 BOTTLE (68788-8438-6)
68788-8438-8 68788-8438 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230428 N/A ANDA ANDA213794 Preferred Pharmaceuticals Inc. IBUPROFEN 400 mg/1 28 TABLET in 1 BOTTLE (68788-8438-8)
68788-8438-9 68788-8438 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230428 N/A ANDA ANDA213794 Preferred Pharmaceuticals Inc. IBUPROFEN 400 mg/1 90 TABLET in 1 BOTTLE (68788-8438-9)
59651-361-01 59651-361 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20200508 N/A ANDA ANDA213794 Aurobindo Pharma Limited IBUPROFEN 600 mg/1 100 TABLET in 1 BOTTLE (59651-361-01)
59651-361-05 59651-361 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20200508 N/A ANDA ANDA213794 Aurobindo Pharma Limited IBUPROFEN 600 mg/1 500 TABLET in 1 BOTTLE (59651-361-05)
68788-8438-2 68788-8438 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230428 N/A ANDA ANDA213794 Preferred Pharmaceuticals Inc. IBUPROFEN 400 mg/1 20 TABLET in 1 BOTTLE (68788-8438-2)
68788-8438-3 68788-8438 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230428 N/A ANDA ANDA213794 Preferred Pharmaceuticals Inc. IBUPROFEN 400 mg/1 30 TABLET in 1 BOTTLE (68788-8438-3)
68788-8438-5 68788-8438 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230428 N/A ANDA ANDA213794 Preferred Pharmaceuticals Inc. IBUPROFEN 400 mg/1 50 TABLET in 1 BOTTLE (68788-8438-5)
70518-4341-0 70518-4341 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250516 N/A ANDA ANDA213794 REMEDYREPACK INC. IBUPROFEN 600 mg/1 30 TABLET in 1 BLISTER PACK (70518-4341-0)
70518-4341-1 70518-4341 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250819 N/A ANDA ANDA213794 REMEDYREPACK INC. IBUPROFEN 600 mg/1 30 TABLET in 1 BLISTER PACK (70518-4341-1)
68071-3696-8 68071-3696 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20241008 N/A ANDA ANDA213794 NuCare Pharmaceuticals, Inc. IBUPROFEN 800 mg/1 180 TABLET in 1 BOTTLE (68071-3696-8)
72603-910-01 72603-910 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20260601 N/A ANDA ANDA213794 NorthStar Rx LLC IBUPROFEN 800 mg/1 100 TABLET in 1 BOTTLE (72603-910-01)
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