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=ANDA090255"
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
76282-309-01 76282-309 HUMAN PRESCRIPTION DRUG HydrALAZINE Hydrochloride HydrALAZINE Hydrochloride TABLET ORAL 20160520 N/A ANDA ANDA090255 Exelan Pharmaceuticals Inc. HYDRALAZINE HYDROCHLORIDE 10 mg/1 100 TABLET in 1 BOTTLE (76282-309-01)
76282-309-10 76282-309 HUMAN PRESCRIPTION DRUG HydrALAZINE Hydrochloride HydrALAZINE Hydrochloride TABLET ORAL 20160520 N/A ANDA ANDA090255 Exelan Pharmaceuticals Inc. HYDRALAZINE HYDROCHLORIDE 10 mg/1 1000 TABLET in 1 BOTTLE (76282-309-10)
76282-310-01 76282-310 HUMAN PRESCRIPTION DRUG HydrALAZINE Hydrochloride HydrALAZINE Hydrochloride TABLET ORAL 20160520 N/A ANDA ANDA090255 Exelan Pharmaceuticals Inc. HYDRALAZINE HYDROCHLORIDE 25 mg/1 100 TABLET in 1 BOTTLE (76282-310-01)
76282-310-10 76282-310 HUMAN PRESCRIPTION DRUG HydrALAZINE Hydrochloride HydrALAZINE Hydrochloride TABLET ORAL 20160520 N/A ANDA ANDA090255 Exelan Pharmaceuticals Inc. HYDRALAZINE HYDROCHLORIDE 25 mg/1 1000 TABLET in 1 BOTTLE (76282-310-10)
76282-311-01 76282-311 HUMAN PRESCRIPTION DRUG HydrALAZINE Hydrochloride HydrALAZINE Hydrochloride TABLET ORAL 20160520 N/A ANDA ANDA090255 Exelan Pharmaceuticals Inc. HYDRALAZINE HYDROCHLORIDE 50 mg/1 100 TABLET in 1 BOTTLE (76282-311-01)
76282-311-10 76282-311 HUMAN PRESCRIPTION DRUG HydrALAZINE Hydrochloride HydrALAZINE Hydrochloride TABLET ORAL 20160520 N/A ANDA ANDA090255 Exelan Pharmaceuticals Inc. HYDRALAZINE HYDROCHLORIDE 50 mg/1 1000 TABLET in 1 BOTTLE (76282-311-10)
76282-312-01 76282-312 HUMAN PRESCRIPTION DRUG HydrALAZINE Hydrochloride HydrALAZINE Hydrochloride TABLET ORAL 20160520 N/A ANDA ANDA090255 Exelan Pharmaceuticals Inc. HYDRALAZINE HYDROCHLORIDE 100 mg/1 100 TABLET in 1 BOTTLE (76282-312-01)
43353-205-05 43353-205 HUMAN PRESCRIPTION DRUG HydrALAZINE Hydrochloride HydrALAZINE Hydrochloride TABLET ORAL 20160709 N/A ANDA ANDA090255 Aphena Pharma Solutions - Tennessee, LLC HYDRALAZINE HYDROCHLORIDE 100 mg/1 4200 TABLET in 1 BOTTLE (43353-205-05)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase