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
71335-2689-1 71335-2689 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250918 N/A ANDA ANDA213794 Bryant Ranch Prepack IBUPROFEN 800 mg/1 20 TABLET in 1 BOTTLE (71335-2689-1)
71335-2689-2 71335-2689 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250918 N/A ANDA ANDA213794 Bryant Ranch Prepack IBUPROFEN 800 mg/1 15 TABLET in 1 BOTTLE (71335-2689-2)
71335-2689-3 71335-2689 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250918 N/A ANDA ANDA213794 Bryant Ranch Prepack IBUPROFEN 800 mg/1 40 TABLET in 1 BOTTLE (71335-2689-3)
71335-2689-4 71335-2689 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250918 N/A ANDA ANDA213794 Bryant Ranch Prepack IBUPROFEN 800 mg/1 21 TABLET in 1 BOTTLE (71335-2689-4)
71335-2689-5 71335-2689 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250918 N/A ANDA ANDA213794 Bryant Ranch Prepack IBUPROFEN 800 mg/1 30 TABLET in 1 BOTTLE (71335-2689-5)
71335-2689-6 71335-2689 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250918 N/A ANDA ANDA213794 Bryant Ranch Prepack IBUPROFEN 800 mg/1 90 TABLET in 1 BOTTLE (71335-2689-6)
71335-2689-7 71335-2689 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250918 N/A ANDA ANDA213794 Bryant Ranch Prepack IBUPROFEN 800 mg/1 100 TABLET in 1 BOTTLE (71335-2689-7)
71335-2689-8 71335-2689 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250918 N/A ANDA ANDA213794 Bryant Ranch Prepack IBUPROFEN 800 mg/1 120 TABLET in 1 BOTTLE (71335-2689-8)
71335-2689-9 71335-2689 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250918 N/A ANDA ANDA213794 Bryant Ranch Prepack IBUPROFEN 800 mg/1 60 TABLET in 1 BOTTLE (71335-2689-9)
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)
83008-066-30 83008-066 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20240708 20270430 ANDA ANDA213794 Quality Care Products, LLC IBUPROFEN 600 mg/1 30 TABLET in 1 BOTTLE (83008-066-30)
83008-066-60 83008-066 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20240708 20270228 ANDA ANDA213794 Quality Care Products, LLC IBUPROFEN 600 mg/1 60 TABLET in 1 BOTTLE (83008-066-60)
76420-576-01 76420-576 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230720 N/A ANDA ANDA213794 Asclemed USA, Inc. IBUPROFEN 600 mg/1 100 TABLET in 1 BOTTLE (76420-576-01)
76420-576-02 76420-576 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20231006 N/A ANDA ANDA213794 Asclemed USA, Inc. IBUPROFEN 600 mg/1 2 TABLET in 1 BOTTLE (76420-576-02)
76420-576-05 76420-576 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20231006 N/A ANDA ANDA213794 Asclemed USA, Inc. IBUPROFEN 600 mg/1 500 TABLET in 1 BOTTLE (76420-576-05)
76420-576-10 76420-576 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20231006 N/A ANDA ANDA213794 Asclemed USA, Inc. IBUPROFEN 600 mg/1 10 TABLET in 1 BOTTLE (76420-576-10)
76420-576-20 76420-576 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20231006 N/A ANDA ANDA213794 Asclemed USA, Inc. IBUPROFEN 600 mg/1 20 TABLET in 1 BOTTLE (76420-576-20)
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