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=ANDA075682"
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
71610-275-60 71610-275 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20190508 N/A ANDA ANDA075682 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 800 mg/1 90 TABLET in 1 BOTTLE (71610-275-60)
71610-275-80 71610-275 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20190508 N/A ANDA ANDA075682 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 800 mg/1 180 TABLET in 1 BOTTLE (71610-275-80)
71610-275-92 71610-275 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20190508 N/A ANDA ANDA075682 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 800 mg/1 270 TABLET in 1 BOTTLE (71610-275-92)
63629-1468-5 63629-1468 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20110429 N/A ANDA ANDA075682 Bryant Ranch Prepack IBUPROFEN 400 mg/1 90 TABLET in 1 BOTTLE (63629-1468-5)
63629-1468-6 63629-1468 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20120926 N/A ANDA ANDA075682 Bryant Ranch Prepack IBUPROFEN 400 mg/1 120 TABLET in 1 BOTTLE (63629-1468-6)
71610-501-92 71610-501 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20201208 N/A ANDA ANDA075682 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 600 mg/1 270 TABLET in 1 BOTTLE (71610-501-92)
68788-9110-1 68788-9110 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Preferred Pharmaceuticals, Inc. IBUPROFEN 400 mg/1 100 TABLET in 1 BOTTLE (68788-9110-1)
55154-0741-0 55154-0741 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20090610 N/A ANDA ANDA075682 Cardinal Health 107, LLC IBUPROFEN 600 mg/1 10 BLISTER PACK in 1 BAG (55154-0741-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
0904-5854-40 0904-5854 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20090610 N/A ANDA ANDA075682 Major Pharmaceuticals IBUPROFEN 600 mg/1 500 TABLET in 1 BOTTLE (0904-5854-40)
0904-5854-60 0904-5854 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20090610 N/A ANDA ANDA075682 Major Pharmaceuticals IBUPROFEN 600 mg/1 100 TABLET in 1 BOTTLE (0904-5854-60)
0904-5854-61 0904-5854 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20090610 N/A ANDA ANDA075682 Major Pharmaceuticals IBUPROFEN 600 mg/1 100 BLISTER PACK in 1 CARTON (0904-5854-61) / 1 TABLET in 1 BLISTER PACK
68788-9110-2 68788-9110 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Preferred Pharmaceuticals, Inc. IBUPROFEN 400 mg/1 20 TABLET in 1 BOTTLE (68788-9110-2)
68788-9110-3 68788-9110 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Preferred Pharmaceuticals, Inc. IBUPROFEN 400 mg/1 30 TABLET in 1 BOTTLE (68788-9110-3)
68788-9110-5 68788-9110 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Preferred Pharmaceuticals, Inc. IBUPROFEN 400 mg/1 50 TABLET in 1 BOTTLE (68788-9110-5)
68788-9110-6 68788-9110 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Preferred Pharmaceuticals, Inc. IBUPROFEN 400 mg/1 60 TABLET in 1 BOTTLE (68788-9110-6)
68788-9110-7 68788-9110 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Preferred Pharmaceuticals, Inc. IBUPROFEN 400 mg/1 21 TABLET in 1 BOTTLE (68788-9110-7)
68788-9110-8 68788-9110 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Preferred Pharmaceuticals, Inc. IBUPROFEN 400 mg/1 120 TABLET in 1 BOTTLE (68788-9110-8)
68788-9110-9 68788-9110 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Preferred Pharmaceuticals, Inc. IBUPROFEN 400 mg/1 90 TABLET in 1 BOTTLE (68788-9110-9)
55111-682-01 55111-682 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Dr. Reddy's Laboratories Limited IBUPROFEN 400 mg/1 100 TABLET in 1 BOTTLE (55111-682-01)
55111-682-05 55111-682 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Dr. Reddy's Laboratories Limited IBUPROFEN 400 mg/1 500 TABLET in 1 BOTTLE (55111-682-05)
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