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=ANDA202413"
符合检索条件的记录共 130 条，共 7 页，当前第 2 页 ，可点击列名称排序
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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
50090-7288-9 50090-7288 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20241008 N/A ANDA ANDA202413 A-S Medication Solutions IBUPROFEN 600 mg/1 24 TABLET, FILM COATED in 1 BOTTLE (50090-7288-9)
50090-7283-8 50090-7283 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20241008 N/A ANDA ANDA202413 A-S Medication Solutions IBUPROFEN 800 mg/1 12 TABLET, FILM COATED in 1 BOTTLE (50090-7283-8)
50090-7283-9 50090-7283 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20241008 N/A ANDA ANDA202413 A-S Medication Solutions IBUPROFEN 800 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (50090-7283-9)
50090-7288-7 50090-7288 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20241008 N/A ANDA ANDA202413 A-S Medication Solutions IBUPROFEN 600 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (50090-7288-7)
50090-7320-0 50090-7320 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20241014 N/A ANDA ANDA202413 A-S Medication Solutions IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-7320-0)
50090-7321-0 50090-7321 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20241015 N/A ANDA ANDA202413 A-S Medication Solutions IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-7321-0)
76420-846-05 76420-846 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 400 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76420-846-05)
76420-846-90 76420-846 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 400 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-846-90)
76420-846-30 76420-846 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 400 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-846-30)
76420-846-60 76420-846 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 400 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-846-60)
76420-846-01 76420-846 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 400 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-846-01)
76420-847-01 76420-847 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 600 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-847-01)
76420-847-90 76420-847 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-847-90)
82804-137-15 82804-137 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20241001 N/A ANDA ANDA202413 Proficient Rx LP IBUPROFEN 400 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (82804-137-15)
82804-137-30 82804-137 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20241024 N/A ANDA ANDA202413 Proficient Rx LP IBUPROFEN 400 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (82804-137-30)
82804-137-60 82804-137 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240830 N/A ANDA ANDA202413 Proficient Rx LP IBUPROFEN 400 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (82804-137-60)
76420-848-01 76420-848 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 800 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-848-01)
76420-848-05 76420-848 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 800 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76420-848-05)
76420-848-30 76420-848 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-848-30)
76420-848-60 76420-848 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 800 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-848-60)
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