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
63187-614-28 63187-614 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20191001 N/A ANDA ANDA075682 Proficient Rx LP IBUPROFEN 600 mg/1 28 TABLET in 1 BOTTLE (63187-614-28)
63187-614-30 63187-614 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20160101 N/A ANDA ANDA075682 Proficient Rx LP IBUPROFEN 600 mg/1 30 TABLET in 1 BOTTLE (63187-614-30)
63187-614-40 63187-614 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20170601 N/A ANDA ANDA075682 Proficient Rx LP IBUPROFEN 600 mg/1 40 TABLET in 1 BOTTLE (63187-614-40)
63187-614-42 63187-614 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20200221 N/A ANDA ANDA075682 Proficient Rx LP IBUPROFEN 600 mg/1 42 TABLET in 1 BOTTLE (63187-614-42)
63187-614-45 63187-614 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20160101 N/A ANDA ANDA075682 Proficient Rx LP IBUPROFEN 600 mg/1 45 TABLET in 1 BOTTLE (63187-614-45)
63187-614-60 63187-614 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20160101 N/A ANDA ANDA075682 Proficient Rx LP IBUPROFEN 600 mg/1 60 TABLET in 1 BOTTLE (63187-614-60)
63187-614-90 63187-614 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20160101 N/A ANDA ANDA075682 Proficient Rx LP IBUPROFEN 600 mg/1 90 TABLET in 1 BOTTLE (63187-614-90)
63187-614-21 63187-614 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20251211 N/A ANDA ANDA075682 Proficient Rx LP IBUPROFEN 600 mg/1 21 TABLET in 1 BOTTLE (63187-614-21)
63187-614-20 63187-614 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20170301 N/A ANDA ANDA075682 Proficient Rx LP IBUPROFEN 600 mg/1 20 TABLET in 1 BOTTLE (63187-614-20)
63187-614-15 63187-614 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20160101 N/A ANDA ANDA075682 Proficient Rx LP IBUPROFEN 600 mg/1 15 TABLET in 1 BOTTLE (63187-614-15)
0904-5853-40 0904-5853 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20090610 N/A ANDA ANDA075682 Major Pharmaceuticals IBUPROFEN 400 mg/1 500 TABLET in 1 BOTTLE (0904-5853-40)
0904-5854-60 0904-5854 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20090610 N/A ANDA ANDA075682 Major Pharmaceuticals IBUPROFEN 600 mg/1 100 TABLET in 1 BOTTLE (0904-5854-60)
0904-5854-61 0904-5854 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20090610 N/A ANDA ANDA075682 Major Pharmaceuticals IBUPROFEN 600 mg/1 100 BLISTER PACK in 1 CARTON (0904-5854-61) / 1 TABLET in 1 BLISTER PACK
0904-5855-40 0904-5855 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20090610 N/A ANDA ANDA075682 Major Pharmaceuticals IBUPROFEN 800 mg/1 500 TABLET in 1 BOTTLE (0904-5855-40)
0904-5855-60 0904-5855 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20090610 N/A ANDA ANDA075682 Major Pharmaceuticals IBUPROFEN 800 mg/1 100 TABLET in 1 BOTTLE (0904-5855-60)
0904-5855-61 0904-5855 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20090610 N/A ANDA ANDA075682 Major Pharmaceuticals IBUPROFEN 800 mg/1 100 BLISTER PACK in 1 CARTON (0904-5855-61) / 1 TABLET in 1 BLISTER PACK
0904-5853-60 0904-5853 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20090610 N/A ANDA ANDA075682 Major Pharmaceuticals IBUPROFEN 400 mg/1 100 TABLET in 1 BOTTLE (0904-5853-60)
0904-5853-61 0904-5853 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20090610 N/A ANDA ANDA075682 Major Pharmaceuticals IBUPROFEN 400 mg/1 100 BLISTER PACK in 1 CARTON (0904-5853-61) / 1 TABLET in 1 BLISTER PACK
0904-5854-40 0904-5854 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20090610 N/A ANDA ANDA075682 Major Pharmaceuticals IBUPROFEN 600 mg/1 500 TABLET in 1 BOTTLE (0904-5854-40)
71610-275-60 71610-275 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20190508 N/A ANDA ANDA075682 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 800 mg/1 90 TABLET in 1 BOTTLE (71610-275-60)
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