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=ANDA090796"
符合检索条件的记录共 147 条，共 8 页，当前第 5 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
68071-4009-6 68071-4009 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170719 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68071-4009-6)
68071-4009-7 68071-4009 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170719 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (68071-4009-7)
68071-4009-9 68071-4009 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170719 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-4009-9)
60760-603-20 60760-603 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191021 N/A ANDA ANDA090796 St. Mary's Medical Park Pharmacy IBUPROFEN 600 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-603-20)
60760-603-28 60760-603 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191210 N/A ANDA ANDA090796 St. Mary's Medical Park Pharmacy IBUPROFEN 600 mg/1 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-603-28)
60760-603-30 60760-603 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20211020 N/A ANDA ANDA090796 St. Mary's Medical Park Pharmacy IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-603-30)
60760-603-40 60760-603 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191226 N/A ANDA ANDA090796 St. Mary's Medical Park Pharmacy IBUPROFEN 600 mg/1 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-603-40)
60760-603-60 60760-603 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191021 N/A ANDA ANDA090796 St. Mary's Medical Park Pharmacy IBUPROFEN 600 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-603-60)
60760-603-90 60760-603 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20230206 N/A ANDA ANDA090796 St. Mary's Medical Park Pharmacy IBUPROFEN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-603-90)
60760-604-09 60760-604 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200610 N/A ANDA ANDA090796 St. Mary's Medical Park Pharmacy IBUPROFEN 800 mg/1 9 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-604-09)
60760-604-20 60760-604 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191016 N/A ANDA ANDA090796 St. Mary's Medical Park Pharmacy IBUPROFEN 800 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-604-20)
60760-604-30 60760-604 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200708 N/A ANDA ANDA090796 St. Mary's Medical Park Pharmacy IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-604-30)
60760-604-60 60760-604 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191016 N/A ANDA ANDA090796 St. Mary's Medical Park Pharmacy IBUPROFEN 800 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-604-60)
60760-604-90 60760-604 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191016 N/A ANDA ANDA090796 St. Mary's Medical Park Pharmacy IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-604-90)
68071-4243-1 68071-4243 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20180122 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68071-4243-1)
68071-4459-6 68071-4459 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20180531 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (68071-4459-6)
68071-4009-1 68071-4009 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170719 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 21 TABLET, FILM COATED in 1 BOTTLE (68071-4009-1)
72189-231-30 72189-231 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20210604 N/A ANDA ANDA090796 DIRECT RX IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72189-231-30)
72189-231-60 72189-231 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20210604 N/A ANDA ANDA090796 DIRECT RX IBUPROFEN 600 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (72189-231-60)
72189-231-90 72189-231 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20210604 N/A ANDA ANDA090796 DIRECT RX IBUPROFEN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (72189-231-90)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase