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
68071-2947-5 68071-2947 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230303 N/A ANDA ANDA213794 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 50 TABLET in 1 BOTTLE (68071-2947-5)
68071-2947-6 68071-2947 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230303 N/A ANDA ANDA213794 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 60 TABLET in 1 BOTTLE (68071-2947-6)
68071-2947-9 68071-2947 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230303 N/A ANDA ANDA213794 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 90 TABLET in 1 BOTTLE (68071-2947-9)
70518-3861-1 70518-3861 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20260511 N/A ANDA ANDA213794 REMEDYREPACK INC. IBUPROFEN 400 mg/1 100 POUCH in 1 BOX, UNIT-DOSE (70518-3861-1) / 1 TABLET in 1 POUCH (70518-3861-2)
50090-6886-0 50090-6886 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20231206 N/A ANDA ANDA213794 A-S Medication Solutions IBUPROFEN 800 mg/1 90 TABLET in 1 BOTTLE (50090-6886-0)
70518-4010-0 70518-4010 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20240205 N/A ANDA ANDA213794 REMEDYREPACK INC. IBUPROFEN 800 mg/1 30 TABLET in 1 BLISTER PACK (70518-4010-0)
70518-4010-2 70518-4010 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250602 N/A ANDA ANDA213794 REMEDYREPACK INC. IBUPROFEN 800 mg/1 30 TABLET in 1 BLISTER PACK (70518-4010-2)
68071-2947-2 68071-2947 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230303 N/A ANDA ANDA213794 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 20 TABLET in 1 BOTTLE (68071-2947-2)
68071-2998-6 68071-2998 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230504 N/A ANDA ANDA213794 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 6 TABLET in 1 BOTTLE (68071-2998-6)
68071-2947-1 68071-2947 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230303 N/A ANDA ANDA213794 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 21 TABLET in 1 BOTTLE (68071-2947-1)
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)
59651-362-01 59651-362 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20200508 N/A ANDA ANDA213794 Aurobindo Pharma Limited IBUPROFEN 800 mg/1 100 TABLET in 1 BOTTLE (59651-362-01)
59651-362-05 59651-362 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20200508 N/A ANDA ANDA213794 Aurobindo Pharma Limited IBUPROFEN 800 mg/1 500 TABLET in 1 BOTTLE (59651-362-05)
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)
59651-360-01 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)
59651-361-05 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)
68071-3442-2 68071-3442 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20241219 N/A ANDA ANDA213794 NuCare Pharmaceuticals,Inc. IBUPROFEN 400 mg/1 20 TABLET in 1 BOTTLE (68071-3442-2)
68071-3442-3 68071-3442 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230620 N/A ANDA ANDA213794 NuCare Pharmaceuticals,Inc. IBUPROFEN 400 mg/1 30 TABLET in 1 BOTTLE (68071-3442-3)
68071-3442-9 68071-3442 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230620 N/A ANDA ANDA213794 NuCare Pharmaceuticals,Inc. IBUPROFEN 400 mg/1 90 TABLET in 1 BOTTLE (68071-3442-9)
68788-8319-2 68788-8319 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20221223 N/A ANDA ANDA213794 Preferred Pharmaceuticals Inc. IBUPROFEN 800 mg/1 20 TABLET in 1 BOTTLE (68788-8319-2)
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