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
60687-446-01 60687-446 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20191001 N/A ANDA ANDA078558 American Health Packaging IBUPROFEN 400 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-446-01) / 1 TABLET in 1 BLISTER PACK (60687-446-11)
60687-457-01 60687-457 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20190603 N/A ANDA ANDA078558 American Health Packaging IBUPROFEN 600 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-457-01) / 1 TABLET in 1 BLISTER PACK (60687-457-11)
85509-1466-3 85509-1466 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20251001 N/A ANDA ANDA078558 PHOENIX RX LLC IBUPROFEN 800 mg/1 30 TABLET in 1 BOTTLE (85509-1466-3)
85509-1466-6 85509-1466 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20251001 N/A ANDA ANDA078558 PHOENIX RX LLC IBUPROFEN 800 mg/1 60 TABLET in 1 BOTTLE (85509-1466-6)
85509-1466-9 85509-1466 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20251001 N/A ANDA ANDA078558 PHOENIX RX LLC IBUPROFEN 800 mg/1 90 TABLET in 1 BOTTLE (85509-1466-9)
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