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
51407-369-05 51407-369 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20210222 N/A ANDA ANDA075682 Golden State Medical Supply, Inc. IBUPROFEN 400 mg/1 500 TABLET in 1 BOTTLE (51407-369-05)
51407-370-05 51407-370 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20210222 N/A ANDA ANDA075682 Golden State Medical Supply, Inc. IBUPROFEN 600 mg/1 500 TABLET in 1 BOTTLE (51407-370-05)
51407-371-05 51407-371 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20210222 N/A ANDA ANDA075682 Golden State Medical Supply, Inc. IBUPROFEN 800 mg/1 500 TABLET in 1 BOTTLE (51407-371-05)
55154-1342-0 55154-1342 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20090610 N/A ANDA ANDA075682 Cardinal Health 107, LLC IBUPROFEN 800 mg/1 10 BLISTER PACK in 1 BAG (55154-1342-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
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
51407-840-01 51407-840 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250926 N/A ANDA ANDA075682 Golden State Medical Supply, Inc. IBUPROFEN 600 mg/1 100 TABLET in 1 BOTTLE (51407-840-01)
51407-841-01 51407-841 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250926 N/A ANDA ANDA075682 Golden State Medical Supply, Inc. IBUPROFEN 800 mg/1 100 TABLET in 1 BOTTLE (51407-841-01)
51407-841-05 51407-841 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250926 N/A ANDA ANDA075682 Golden State Medical Supply, Inc. IBUPROFEN 800 mg/1 500 TABLET in 1 BOTTLE (51407-841-05)
55154-1380-0 55154-1380 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20090610 N/A ANDA ANDA075682 Cardinal Health 107, LLC IBUPROFEN 400 mg/1 10 BLISTER PACK in 1 BAG (55154-1380-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
51407-839-01 51407-839 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250926 N/A ANDA ANDA075682 Golden State Medical Supply, Inc. IBUPROFEN 400 mg/1 100 TABLET in 1 BOTTLE (51407-839-01)
51407-839-05 51407-839 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250926 N/A ANDA ANDA075682 Golden State Medical Supply, Inc. IBUPROFEN 400 mg/1 500 TABLET in 1 BOTTLE (51407-839-05)
67296-0913-1 67296-0913 HUMAN PRESCRIPTION DRUG IBU IBU TABLET ORAL 20081120 N/A ANDA ANDA075682 RedPharm Drug, Inc. IBUPROFEN 600 mg/1 30 TABLET in 1 BOTTLE (67296-0913-1)
67296-0913-3 67296-0913 HUMAN PRESCRIPTION DRUG IBU IBU TABLET ORAL 20081120 N/A ANDA ANDA075682 RedPharm Drug, Inc. IBUPROFEN 600 mg/1 10 TABLET in 1 BOTTLE (67296-0913-3)
67296-0913-9 67296-0913 HUMAN PRESCRIPTION DRUG IBU IBU TABLET ORAL 20081120 N/A ANDA ANDA075682 RedPharm Drug, Inc. IBUPROFEN 600 mg/1 90 TABLET in 1 BOTTLE (67296-0913-9)
51407-840-05 51407-840 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20250926 N/A ANDA ANDA075682 Golden State Medical Supply, Inc. IBUPROFEN 600 mg/1 500 TABLET in 1 BOTTLE (51407-840-05)
66267-963-00 66267-963 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20170915 N/A ANDA ANDA075682 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 100 TABLET in 1 BOTTLE (66267-963-00)
66267-964-00 66267-964 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20170822 N/A ANDA ANDA075682 NuCare Pharmaceuticals Inc. IBUPROFEN 600 mg/1 100 TABLET in 1 BOTTLE (66267-964-00)
68071-3053-2 68071-3053 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20180316 N/A ANDA ANDA075682 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 20 TABLET in 1 BOTTLE (68071-3053-2)
68071-3053-6 68071-3053 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20180316 N/A ANDA ANDA075682 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 60 TABLET in 1 BOTTLE (68071-3053-6)
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)
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