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=NDA216834"
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
50474-991-80 50474-991 HUMAN PRESCRIPTION DRUG ZILBRYSQ zilucoplan INJECTION, SOLUTION SUBCUTANEOUS 20240103 N/A NDA NDA216834 UCB, Inc. ZILUCOPLAN 40 mg/mL 4 CARTON in 1 BOX (50474-991-80) / 7 SYRINGE, GLASS in 1 CARTON / .574 mL in 1 SYRINGE, GLASS
50474-992-80 50474-992 HUMAN PRESCRIPTION DRUG ZILBRYSQ zilucoplan INJECTION, SOLUTION SUBCUTANEOUS 20240103 N/A NDA NDA216834 UCB, Inc. ZILUCOPLAN 40 mg/mL 4 CARTON in 1 BOX (50474-992-80) / 7 SYRINGE, GLASS in 1 CARTON / .81 mL in 1 SYRINGE, GLASS
50474-990-80 50474-990 HUMAN PRESCRIPTION DRUG ZILBRYSQ zilucoplan INJECTION, SOLUTION SUBCUTANEOUS 20240315 N/A NDA NDA216834 UCB, Inc. ZILUCOPLAN 40 mg/mL 4 CARTON in 1 BOX (50474-990-80) / 7 SYRINGE, GLASS in 1 CARTON / .416 mL in 1 SYRINGE, GLASS
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