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
71335-2683-2 71335-2683 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250917 N/A ANDA ANDA213794 Bryant Ranch Prepack IBUPROFEN 600 mg/1 15 TABLET in 1 BOTTLE (71335-2683-2)
71335-2683-3 71335-2683 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250917 N/A ANDA ANDA213794 Bryant Ranch Prepack IBUPROFEN 600 mg/1 30 TABLET in 1 BOTTLE (71335-2683-3)
71335-2683-4 71335-2683 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250917 N/A ANDA ANDA213794 Bryant Ranch Prepack IBUPROFEN 600 mg/1 40 TABLET in 1 BOTTLE (71335-2683-4)
71335-2683-5 71335-2683 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250917 N/A ANDA ANDA213794 Bryant Ranch Prepack IBUPROFEN 600 mg/1 60 TABLET in 1 BOTTLE (71335-2683-5)
71335-2683-6 71335-2683 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250917 N/A ANDA ANDA213794 Bryant Ranch Prepack IBUPROFEN 600 mg/1 90 TABLET in 1 BOTTLE (71335-2683-6)
71335-2683-7 71335-2683 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250917 N/A ANDA ANDA213794 Bryant Ranch Prepack IBUPROFEN 600 mg/1 120 TABLET in 1 BOTTLE (71335-2683-7)
71335-2683-8 71335-2683 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250917 N/A ANDA ANDA213794 Bryant Ranch Prepack IBUPROFEN 600 mg/1 50 TABLET in 1 BOTTLE (71335-2683-8)
50090-5433-4 50090-5433 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20210118 N/A ANDA ANDA213794 A-S Medication Solutions IBUPROFEN 600 mg/1 28 TABLET in 1 BOTTLE (50090-5433-4)
50090-6677-0 50090-6677 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230905 N/A ANDA ANDA213794 A-S Medication Solutions IBUPROFEN 400 mg/1 90 TABLET in 1 BOTTLE (50090-6677-0)
50090-6677-2 50090-6677 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230905 N/A ANDA ANDA213794 A-S Medication Solutions IBUPROFEN 400 mg/1 28 TABLET in 1 BOTTLE (50090-6677-2)
76420-577-01 76420-577 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230720 N/A ANDA ANDA213794 Asclemed USA, Inc. IBUPROFEN 800 mg/1 100 TABLET in 1 BOTTLE (76420-577-01)
76420-577-30 76420-577 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230720 N/A ANDA ANDA213794 Asclemed USA, Inc. IBUPROFEN 800 mg/1 30 TABLET in 1 BOTTLE (76420-577-30)
76420-577-60 76420-577 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230720 N/A ANDA ANDA213794 Asclemed USA, Inc. IBUPROFEN 800 mg/1 60 TABLET in 1 BOTTLE (76420-577-60)
76420-577-90 76420-577 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230720 N/A ANDA ANDA213794 Asclemed USA, Inc. IBUPROFEN 800 mg/1 90 TABLET in 1 BOTTLE (76420-577-90)
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)
50090-5433-5 50090-5433 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20210118 N/A ANDA ANDA213794 A-S Medication Solutions IBUPROFEN 600 mg/1 90 TABLET in 1 BOTTLE (50090-5433-5)
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)
50090-6676-0 50090-6676 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230905 N/A ANDA ANDA213794 A-S Medication Solutions IBUPROFEN 400 mg/1 16 TABLET in 1 BOTTLE (50090-6676-0)
50090-6676-1 50090-6676 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230905 N/A ANDA ANDA213794 A-S Medication Solutions IBUPROFEN 400 mg/1 30 TABLET in 1 BOTTLE (50090-6676-1)
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