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
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)
68071-4009-2 68071-4009 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170719 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (68071-4009-2)
68071-4009-3 68071-4009 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170719 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-4009-3)
68071-4009-4 68071-4009 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170719 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (68071-4009-4)
68071-4009-5 68071-4009 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170719 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (68071-4009-5)
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)
68071-5140-3 68071-5140 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20191231 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 3 TABLET, FILM COATED in 1 BOTTLE (68071-5140-3)
80425-0243-4 80425-0243 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230110 N/A ANDA ANDA090796 Advanced Rx Pharmacy of Tennessee, LLC IBUPROFEN 800 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (80425-0243-4)
71335-1503-0 71335-1503 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 600 mg/1 21 TABLET, FILM COATED in 1 BOTTLE (71335-1503-0)
71335-1503-1 71335-1503 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 600 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-1503-1)
71335-1503-2 71335-1503 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 600 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71335-1503-2)
71335-1503-3 71335-1503 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1503-3)
71335-1503-4 71335-1503 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 600 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (71335-1503-4)
71335-1503-5 71335-1503 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 600 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-1503-5)
71335-1503-6 71335-1503 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-1503-6)
71335-1503-7 71335-1503 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200212 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 600 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-1503-7)
68071-5140-6 68071-5140 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200106 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (68071-5140-6)
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)
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