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=ANDA040751"
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
82804-957-90 82804-957 HUMAN PRESCRIPTION DRUG Imipramine Hydrochloride Imipramine Hydrochloride TABLET ORAL 20260112 N/A ANDA ANDA040751 Proficient Rx LP IMIPRAMINE HYDROCHLORIDE 25 mg/1 90 TABLET in 1 BOTTLE (82804-957-90)
82804-958-00 82804-958 HUMAN PRESCRIPTION DRUG Imipramine Hydrochloride Imipramine Hydrochloride TABLET ORAL 20260112 N/A ANDA ANDA040751 Proficient Rx LP IMIPRAMINE HYDROCHLORIDE 50 mg/1 100 TABLET in 1 BOTTLE (82804-958-00)
82804-958-11 82804-958 HUMAN PRESCRIPTION DRUG Imipramine Hydrochloride Imipramine Hydrochloride TABLET ORAL 20260112 N/A ANDA ANDA040751 Proficient Rx LP IMIPRAMINE HYDROCHLORIDE 50 mg/1 1000 TABLET in 1 BOTTLE (82804-958-11)
82804-958-30 82804-958 HUMAN PRESCRIPTION DRUG Imipramine Hydrochloride Imipramine Hydrochloride TABLET ORAL 20260112 N/A ANDA ANDA040751 Proficient Rx LP IMIPRAMINE HYDROCHLORIDE 50 mg/1 30 TABLET in 1 BOTTLE (82804-958-30)
82804-958-55 82804-958 HUMAN PRESCRIPTION DRUG Imipramine Hydrochloride Imipramine Hydrochloride TABLET ORAL 20260112 N/A ANDA ANDA040751 Proficient Rx LP IMIPRAMINE HYDROCHLORIDE 50 mg/1 500 TABLET in 1 BOTTLE (82804-958-55)
82804-958-60 82804-958 HUMAN PRESCRIPTION DRUG Imipramine Hydrochloride Imipramine Hydrochloride TABLET ORAL 20260112 N/A ANDA ANDA040751 Proficient Rx LP IMIPRAMINE HYDROCHLORIDE 50 mg/1 60 TABLET in 1 BOTTLE (82804-958-60)
82804-958-72 82804-958 HUMAN PRESCRIPTION DRUG Imipramine Hydrochloride Imipramine Hydrochloride TABLET ORAL 20260112 N/A ANDA ANDA040751 Proficient Rx LP IMIPRAMINE HYDROCHLORIDE 50 mg/1 120 TABLET in 1 BOTTLE (82804-958-72)
82804-958-90 82804-958 HUMAN PRESCRIPTION DRUG Imipramine Hydrochloride Imipramine Hydrochloride TABLET ORAL 20260112 N/A ANDA ANDA040751 Proficient Rx LP IMIPRAMINE HYDROCHLORIDE 50 mg/1 90 TABLET in 1 BOTTLE (82804-958-90)
72789-240-01 72789-240 HUMAN PRESCRIPTION DRUG Imipramine Hydrochloride Imipramine Hydrochloride TABLET ORAL 20220520 N/A ANDA ANDA040751 PD-Rx Pharmaceuticals, Inc. IMIPRAMINE HYDROCHLORIDE 10 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (72789-240-01)
72789-240-95 72789-240 HUMAN PRESCRIPTION DRUG Imipramine Hydrochloride Imipramine Hydrochloride TABLET ORAL 20220415 N/A ANDA ANDA040751 PD-Rx Pharmaceuticals, Inc. IMIPRAMINE HYDROCHLORIDE 10 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (72789-240-95)
72789-243-01 72789-243 HUMAN PRESCRIPTION DRUG Imipramine Hydrochloride Imipramine Hydrochloride TABLET ORAL 20220414 N/A ANDA ANDA040751 PD-Rx Pharmaceuticals, Inc. IMIPRAMINE HYDROCHLORIDE 25 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (72789-243-01)
72789-243-95 72789-243 HUMAN PRESCRIPTION DRUG Imipramine Hydrochloride Imipramine Hydrochloride TABLET ORAL 20221128 N/A ANDA ANDA040751 PD-Rx Pharmaceuticals, Inc. IMIPRAMINE HYDROCHLORIDE 25 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (72789-243-95)
72789-244-01 72789-244 HUMAN PRESCRIPTION DRUG Imipramine Hydrochloride Imipramine Hydrochloride TABLET ORAL 20220414 N/A ANDA ANDA040751 PD-Rx Pharmaceuticals, Inc. IMIPRAMINE HYDROCHLORIDE 50 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (72789-244-01)
72789-244-95 72789-244 HUMAN PRESCRIPTION DRUG Imipramine Hydrochloride Imipramine Hydrochloride TABLET ORAL 20221128 N/A ANDA ANDA040751 PD-Rx Pharmaceuticals, Inc. IMIPRAMINE HYDROCHLORIDE 50 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (72789-244-95)
80425-0342-1 80425-0342 HUMAN PRESCRIPTION DRUG Imipramine Hydrochloride Imipramine Hydrochloride TABLET, FILM COATED ORAL 20230606 N/A ANDA ANDA040751 Advanced Rx Pharmacy of Tennessee, LLC IMIPRAMINE HYDROCHLORIDE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (80425-0342-1)
80425-0342-2 80425-0342 HUMAN PRESCRIPTION DRUG Imipramine Hydrochloride Imipramine Hydrochloride TABLET, FILM COATED ORAL 20230606 N/A ANDA ANDA040751 Advanced Rx Pharmacy of Tennessee, LLC IMIPRAMINE HYDROCHLORIDE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (80425-0342-2)
80425-0342-3 80425-0342 HUMAN PRESCRIPTION DRUG Imipramine Hydrochloride Imipramine Hydrochloride TABLET, FILM COATED ORAL 20230606 N/A ANDA ANDA040751 Advanced Rx Pharmacy of Tennessee, LLC IMIPRAMINE HYDROCHLORIDE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (80425-0342-3)
70868-810-10 70868-810 HUMAN PRESCRIPTION DRUG Imipramine Hydrochloride Imipramine Hydrochloride TABLET, FILM COATED ORAL 20220718 N/A ANDA ANDA040751 Key Therapeutics IMIPRAMINE HYDROCHLORIDE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70868-810-10)
68071-3669-9 68071-3669 HUMAN PRESCRIPTION DRUG Imipramine Hydrochloride Imipramine Hydrochloride TABLET ORAL 20200801 N/A ANDA ANDA040751 NuCare Pharmaceuticals, Inc. IMIPRAMINE HYDROCHLORIDE 50 mg/1 90 TABLET in 1 BOTTLE (68071-3669-9)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase