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"
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
72189-266-72 72189-266 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20210916 N/A ANDA ANDA090796 DIRECT RX IBUPROFEN 800 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (72189-266-72)
72189-266-90 72189-266 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20210916 N/A ANDA ANDA090796 DIRECT RX IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (72189-266-90)
25000-122-03 25000-122 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20110228 N/A ANDA ANDA090796 MARKSANS PHARMA LIMITED IBUPROFEN 600 mg/1 30 TABLET in 1 BOTTLE (25000-122-03)
25000-122-12 25000-122 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20110228 N/A ANDA ANDA090796 MARKSANS PHARMA LIMITED IBUPROFEN 600 mg/1 500 TABLET in 1 BOTTLE (25000-122-12)
42708-097-30 42708-097 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20190531 N/A ANDA ANDA090796 QPharma, Inc. IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (42708-097-30)
51655-474-20 51655-474 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20201119 N/A ANDA ANDA090796 Northwind Health Company, LLC IBUPROFEN 600 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-474-20)
51655-474-25 51655-474 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20201113 N/A ANDA ANDA090796 Northwind Health Company, LLC IBUPROFEN 600 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-474-25)
51655-474-26 51655-474 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220621 N/A ANDA ANDA090796 Northwind Health Company, LLC IBUPROFEN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-474-26)
51655-474-51 51655-474 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20210208 N/A ANDA ANDA090796 Northwind Health Company, LLC IBUPROFEN 600 mg/1 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-474-51)
51655-474-52 51655-474 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20210114 N/A ANDA ANDA090796 Northwind Health Company, LLC IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-474-52)
43063-867-01 43063-867 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20180711 N/A ANDA ANDA090796 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 600 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-867-01)
43063-867-10 43063-867 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20180905 N/A ANDA ANDA090796 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 600 mg/1 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-867-10)
68071-3362-0 68071-3362 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170726 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 12 TABLET, FILM COATED in 1 BOTTLE (68071-3362-0)
68071-3362-1 68071-3362 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170726 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 21 TABLET, FILM COATED in 1 BOTTLE (68071-3362-1)
49483-604-01 49483-604 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151230 N/A ANDA ANDA090796 TIME CAP LABORATORIES, INC IBUPROFEN 800 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (49483-604-01)
49483-604-03 49483-604 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151230 N/A ANDA ANDA090796 TIME CAP LABORATORIES, INC IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (49483-604-03)
80425-0089-1 80425-0089 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151230 N/A ANDA ANDA090796 Advanced Rx of Tennessee, LLC IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (80425-0089-1)
80425-0089-2 80425-0089 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151230 N/A ANDA ANDA090796 Advanced Rx of Tennessee, LLC IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (80425-0089-2)
80425-0089-3 80425-0089 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151230 N/A ANDA ANDA090796 Advanced Rx of Tennessee, LLC IBUPROFEN 800 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (80425-0089-3)
80425-0089-4 80425-0089 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151230 N/A ANDA ANDA090796 Advanced Rx of Tennessee, LLC IBUPROFEN 800 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (80425-0089-4)
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