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=ANDA205008"
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
71335-2297-2 71335-2297 HUMAN PRESCRIPTION DRUG Phentermine hydrochloride phentermine hydrochloride TABLET ORAL 20250131 N/A ANDA ANDA205008 Bryant Ranch Prepack PHENTERMINE HYDROCHLORIDE 37.5 mg/1 100 TABLET in 1 BOTTLE (71335-2297-2)
63629-2389-1 63629-2389 HUMAN PRESCRIPTION DRUG Phentermine hydrochloride phentermine hydrochloride TABLET ORAL 20170124 N/A ANDA ANDA205008 Bryant Ranch Prepack PHENTERMINE HYDROCHLORIDE 37.5 mg/1 100 TABLET in 1 BOTTLE (63629-2389-1)
45865-222-30 45865-222 HUMAN PRESCRIPTION DRUG Phentermine hydrochloride phentermine hydrochloride TABLET ORAL 20220726 N/A ANDA ANDA205008 Medsource Pharmaceuticals PHENTERMINE HYDROCHLORIDE 37.5 mg/1 30 TABLET in 1 BOTTLE (45865-222-30)
63629-2388-1 63629-2388 HUMAN PRESCRIPTION DRUG Phentermine hydrochloride phentermine hydrochloride TABLET ORAL 20170124 N/A ANDA ANDA205008 Bryant Ranch Prepack PHENTERMINE HYDROCHLORIDE 37.5 mg/1 1000 TABLET in 1 BOTTLE (63629-2388-1)
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