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
72189-266-15 72189-266 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20210916 N/A ANDA ANDA090796 DIRECT RX IBUPROFEN 800 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (72189-266-15)
72189-266-30 72189-266 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20210916 N/A ANDA ANDA090796 DIRECT RX IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72189-266-30)
71335-1517-1 71335-1517 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200220 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 400 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-1517-1)
71335-1517-2 71335-1517 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200220 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 400 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1517-2)
71335-1517-3 71335-1517 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200220 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 400 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (71335-1517-3)
71335-1517-4 71335-1517 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200220 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 400 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-1517-4)
71335-1517-5 71335-1517 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200220 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 400 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-1517-5)
80425-0393-4 80425-0393 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20240523 N/A ANDA ANDA090796 Advanced Rx of Tennessee, LLC IBUPROFEN 800 mg/1 100 TABLET in 1 BOTTLE (80425-0393-4)
80425-0393-5 80425-0393 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20240523 N/A ANDA ANDA090796 Advanced Rx of Tennessee, LLC IBUPROFEN 800 mg/1 120 TABLET in 1 BOTTLE (80425-0393-5)
71610-532-60 71610-532 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20210309 N/A ANDA ANDA090796 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71610-532-60)
71610-532-80 71610-532 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20210309 N/A ANDA ANDA090796 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 600 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71610-532-80)
71610-532-92 71610-532 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20210309 N/A ANDA ANDA090796 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 600 mg/1 270 TABLET, FILM COATED in 1 BOTTLE (71610-532-92)
25000-121-03 25000-121 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20110228 N/A ANDA ANDA090796 MARKSANS PHARMA LIMITED IBUPROFEN 400 mg/1 30 TABLET in 1 BOTTLE (25000-121-03)
25000-121-12 25000-121 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET ORAL 20110228 N/A ANDA ANDA090796 MARKSANS PHARMA LIMITED IBUPROFEN 400 mg/1 500 TABLET in 1 BOTTLE (25000-121-12)
68071-5134-6 68071-5134 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191213 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 400 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (68071-5134-6)
51655-275-20 51655-275 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20210709 N/A ANDA ANDA090796 Northwind Health Company, LLC IBUPROFEN 800 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-20)
71335-1517-6 71335-1517 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200220 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 400 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-1517-6)
71335-1517-7 71335-1517 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200220 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 400 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-1517-7)
71335-1517-8 71335-1517 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200220 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 400 mg/1 21 TABLET, FILM COATED in 1 BOTTLE (71335-1517-8)
71335-1517-9 71335-1517 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200220 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 400 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71335-1517-9)
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