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=ANDA085588"
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
69543-410-10 69543-410 HUMAN PRESCRIPTION DRUG PHENDIMETRAZINE TARTRATE PHENDIMETRAZINE TARTRATE TABLET ORAL 20180701 N/A ANDA ANDA085588 Virtus Pharmaceuticals, LLC PHENDIMETRAZINE TARTRATE 35 mg/1 100 TABLET in 1 BOTTLE (69543-410-10)
69543-410-11 69543-410 HUMAN PRESCRIPTION DRUG PHENDIMETRAZINE TARTRATE PHENDIMETRAZINE TARTRATE TABLET ORAL 20180701 20260930 ANDA ANDA085588 Virtus Pharmaceuticals, LLC PHENDIMETRAZINE TARTRATE 35 mg/1 1000 TABLET in 1 BOTTLE (69543-410-11)
71335-1840-0 71335-1840 HUMAN PRESCRIPTION DRUG PHENDIMETRAZINE TARTRATE PHENDIMETRAZINE TARTRATE TABLET ORAL 20250130 N/A ANDA ANDA085588 Bryant Ranch Prepack PHENDIMETRAZINE TARTRATE 35 mg/1 120 TABLET in 1 BOTTLE (71335-1840-0)
71335-1840-1 71335-1840 HUMAN PRESCRIPTION DRUG PHENDIMETRAZINE TARTRATE PHENDIMETRAZINE TARTRATE TABLET ORAL 20250130 N/A ANDA ANDA085588 Bryant Ranch Prepack PHENDIMETRAZINE TARTRATE 35 mg/1 30 TABLET in 1 BOTTLE (71335-1840-1)
71335-1840-2 71335-1840 HUMAN PRESCRIPTION DRUG PHENDIMETRAZINE TARTRATE PHENDIMETRAZINE TARTRATE TABLET ORAL 20250130 N/A ANDA ANDA085588 Bryant Ranch Prepack PHENDIMETRAZINE TARTRATE 35 mg/1 90 TABLET in 1 BOTTLE (71335-1840-2)
71335-1840-3 71335-1840 HUMAN PRESCRIPTION DRUG PHENDIMETRAZINE TARTRATE PHENDIMETRAZINE TARTRATE TABLET ORAL 20250130 N/A ANDA ANDA085588 Bryant Ranch Prepack PHENDIMETRAZINE TARTRATE 35 mg/1 15 TABLET in 1 BOTTLE (71335-1840-3)
71335-1840-4 71335-1840 HUMAN PRESCRIPTION DRUG PHENDIMETRAZINE TARTRATE PHENDIMETRAZINE TARTRATE TABLET ORAL 20250130 N/A ANDA ANDA085588 Bryant Ranch Prepack PHENDIMETRAZINE TARTRATE 35 mg/1 60 TABLET in 1 BOTTLE (71335-1840-4)
71335-1840-5 71335-1840 HUMAN PRESCRIPTION DRUG PHENDIMETRAZINE TARTRATE PHENDIMETRAZINE TARTRATE TABLET ORAL 20250130 N/A ANDA ANDA085588 Bryant Ranch Prepack PHENDIMETRAZINE TARTRATE 35 mg/1 7 TABLET in 1 BOTTLE (71335-1840-5)
71335-1840-6 71335-1840 HUMAN PRESCRIPTION DRUG PHENDIMETRAZINE TARTRATE PHENDIMETRAZINE TARTRATE TABLET ORAL 20250130 N/A ANDA ANDA085588 Bryant Ranch Prepack PHENDIMETRAZINE TARTRATE 35 mg/1 21 TABLET in 1 BOTTLE (71335-1840-6)
71335-1840-7 71335-1840 HUMAN PRESCRIPTION DRUG PHENDIMETRAZINE TARTRATE PHENDIMETRAZINE TARTRATE TABLET ORAL 20250130 N/A ANDA ANDA085588 Bryant Ranch Prepack PHENDIMETRAZINE TARTRATE 35 mg/1 42 TABLET in 1 BOTTLE (71335-1840-7)
71335-1840-8 71335-1840 HUMAN PRESCRIPTION DRUG PHENDIMETRAZINE TARTRATE PHENDIMETRAZINE TARTRATE TABLET ORAL 20250130 N/A ANDA ANDA085588 Bryant Ranch Prepack PHENDIMETRAZINE TARTRATE 35 mg/1 100 TABLET in 1 BOTTLE (71335-1840-8)
71335-1840-9 71335-1840 HUMAN PRESCRIPTION DRUG PHENDIMETRAZINE TARTRATE PHENDIMETRAZINE TARTRATE TABLET ORAL 20250130 N/A ANDA ANDA085588 Bryant Ranch Prepack PHENDIMETRAZINE TARTRATE 35 mg/1 28 TABLET in 1 BOTTLE (71335-1840-9)
63629-2489-1 63629-2489 HUMAN PRESCRIPTION DRUG PHENDIMETRAZINE TARTRATE PHENDIMETRAZINE TARTRATE TABLET ORAL 20180701 N/A ANDA ANDA085588 Bryant Ranch Prepack PHENDIMETRAZINE TARTRATE 35 mg/1 1000 TABLET in 1 BOTTLE (63629-2489-1)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase