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=ANDA217334"
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
71335-2892-3 71335-2892 HUMAN PRESCRIPTION DRUG Estradiol Estradiol TABLET ORAL 20251028 N/A ANDA ANDA217334 Bryant Ranch Prepack ESTRADIOL .5 mg/1 90 TABLET in 1 BOTTLE (71335-2892-3)
71335-2892-4 71335-2892 HUMAN PRESCRIPTION DRUG Estradiol Estradiol TABLET ORAL 20251028 N/A ANDA ANDA217334 Bryant Ranch Prepack ESTRADIOL .5 mg/1 60 TABLET in 1 BOTTLE (71335-2892-4)
70954-566-10 70954-566 HUMAN PRESCRIPTION DRUG Estradiol Estradiol TABLET ORAL 20230906 N/A ANDA ANDA217334 ANI Pharmaceuticals, Inc. ESTRADIOL 2 mg/1 100 TABLET in 1 BOTTLE (70954-566-10)
70954-566-20 70954-566 HUMAN PRESCRIPTION DRUG Estradiol Estradiol TABLET ORAL 20230906 N/A ANDA ANDA217334 ANI Pharmaceuticals, Inc. ESTRADIOL 2 mg/1 500 TABLET in 1 BOTTLE (70954-566-20)
70954-565-20 70954-565 HUMAN PRESCRIPTION DRUG Estradiol Estradiol TABLET ORAL 20230906 N/A ANDA ANDA217334 ANI Pharmaceuticals, Inc. ESTRADIOL 1 mg/1 500 TABLET in 1 BOTTLE (70954-565-20)
67046-1568-3 67046-1568 HUMAN PRESCRIPTION DRUG Estradiol Estradiol TABLET ORAL 20250617 N/A ANDA ANDA217334 Coupler LLC ESTRADIOL .5 mg/1 30 TABLET in 1 BLISTER PACK (67046-1568-3)
72789-489-30 72789-489 HUMAN PRESCRIPTION DRUG Estradiol Estradiol TABLET ORAL 20250220 N/A ANDA ANDA217334 PD-Rx Pharmaceuticals, Inc. ESTRADIOL .5 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (72789-489-30)
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