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
68071-3552-3 68071-3552 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20231207 N/A ANDA ANDA213794 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 3 TABLET in 1 BOTTLE (68071-3552-3)
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)
60760-929-20 60760-929 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20231117 N/A ANDA ANDA213794 ST. MARY'S MEDICAL PARK PHARMACY IBUPROFEN 800 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (60760-929-20)
60760-929-30 60760-929 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250223 N/A ANDA ANDA213794 ST. MARY'S MEDICAL PARK PHARMACY IBUPROFEN 800 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (60760-929-30)
60760-929-60 60760-929 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20240223 N/A ANDA ANDA213794 ST. MARY'S MEDICAL PARK PHARMACY IBUPROFEN 800 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (60760-929-60)
60760-929-90 60760-929 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230104 N/A ANDA ANDA213794 ST. MARY'S MEDICAL PARK PHARMACY IBUPROFEN 800 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (60760-929-90)
68788-8354-6 68788-8354 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230210 N/A ANDA ANDA213794 Preferred Pharmaceuticals Inc. IBUPROFEN 600 mg/1 60 TABLET in 1 BOTTLE (68788-8354-6)
68788-8354-7 68788-8354 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20230210 N/A ANDA ANDA213794 Preferred Pharmaceuticals Inc. IBUPROFEN 600 mg/1 21 TABLET in 1 BOTTLE (68788-8354-7)
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)
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)
72189-564-30 72189-564 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20240627 N/A ANDA ANDA213794 Direct_rx IBUPROFEN 400 mg/1 30 TABLET in 1 BOTTLE (72189-564-30)
72189-564-60 72189-564 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20240627 N/A ANDA ANDA213794 Direct_rx IBUPROFEN 400 mg/1 60 TABLET in 1 BOTTLE (72189-564-60)
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)
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)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase