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=ANDA078558"
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
63187-527-72 63187-527 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20150803 N/A ANDA ANDA078558 Proficient Rx LP IBUPROFEN 600 mg/1 120 TABLET in 1 BOTTLE (63187-527-72)
63187-527-90 63187-527 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20150803 N/A ANDA ANDA078558 Proficient Rx LP IBUPROFEN 600 mg/1 90 TABLET in 1 BOTTLE (63187-527-90)
60687-468-01 60687-468 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20200325 N/A ANDA ANDA078558 American Health Packaging IBUPROFEN 800 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-468-01) / 1 TABLET in 1 BLISTER PACK (60687-468-11)
83209-464-60 83209-464 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20240603 N/A ANDA ANDA078558 Boswell Pharmacy Services LLC d/b/a BPS Wholesale IBUPROFEN 400 mg/1 60 TABLET in 1 BLISTER PACK (83209-464-60)
63629-1470-9 63629-1470 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20211221 N/A ANDA ANDA078558 Bryant Ranch Prepack IBUPROFEN 800 mg/1 60 TABLET in 1 BOTTLE (63629-1470-9)
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