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=ANDA074431"
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
63629-8338-1 63629-8338 HUMAN PRESCRIPTION DRUG Flurbiprofen Flurbiprofen TABLET, FILM COATED ORAL 20211223 N/A ANDA ANDA074431 Bryant Ranch Prepack FLURBIPROFEN 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63629-8338-1)
63629-8338-2 63629-8338 HUMAN PRESCRIPTION DRUG Flurbiprofen Flurbiprofen TABLET, FILM COATED ORAL 20200717 N/A ANDA ANDA074431 Bryant Ranch Prepack FLURBIPROFEN 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63629-8338-2)
63629-8808-1 63629-8808 HUMAN PRESCRIPTION DRUG Flurbiprofen Flurbiprofen TABLET, FILM COATED ORAL 19950602 N/A ANDA ANDA074431 Bryant Ranch Prepack FLURBIPROFEN 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (63629-8808-1)
64950-218-03 64950-218 HUMAN PRESCRIPTION DRUG Flurbiprofen Flurbiprofen TABLET ORAL 20241101 N/A ANDA ANDA074431 Genus Lifesciences FLURBIPROFEN 100 mg/1 30 TABLET in 1 BOTTLE (64950-218-03)
64950-218-10 64950-218 HUMAN PRESCRIPTION DRUG Flurbiprofen Flurbiprofen TABLET ORAL 20241101 N/A ANDA ANDA074431 Genus Lifesciences FLURBIPROFEN 100 mg/1 100 TABLET in 1 BOTTLE (64950-218-10)
71085-082-30 71085-082 HUMAN PRESCRIPTION DRUG LURBIRO Flurbiprofen TABLET ORAL 20250801 N/A ANDA ANDA074431 IPG Pharmaceuticals, Inc. FLURBIPROFEN 100 mg/1 30 TABLET in 1 BOTTLE (71085-082-30)
68071-4436-4 68071-4436 HUMAN PRESCRIPTION DRUG Flurbiprofen Flurbiprofen TABLET, FILM COATED ORAL 20180517 N/A ANDA ANDA074431 NuCare Pharmaceuticals,Inc. FLURBIPROFEN 100 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (68071-4436-4)
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