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=ANDA217945"
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
71288-731-53 71288-731 HUMAN PRESCRIPTION DRUG propofol propofol INJECTION, EMULSION INTRAVENOUS 20251202 N/A ANDA ANDA217945 Meitheal Pharmaceuticals Inc. PROPOFOL 10 mg/mL 10 VIAL in 1 CARTON (71288-731-53) / 100 mL in 1 VIAL (71288-731-52)
71288-730-51 71288-730 HUMAN PRESCRIPTION DRUG propofol propofol INJECTION, EMULSION INTRAVENOUS 20251202 N/A ANDA ANDA217945 Meitheal Pharmaceuticals Inc. PROPOFOL 10 mg/mL 10 VIAL in 1 CARTON (71288-730-51) / 50 mL in 1 VIAL (71288-730-50)
71288-729-21 71288-729 HUMAN PRESCRIPTION DRUG propofol propofol INJECTION, EMULSION INTRAVENOUS 20251202 N/A ANDA ANDA217945 Meitheal Pharmaceuticals Inc. PROPOFOL 10 mg/mL 10 VIAL in 1 CARTON (71288-729-21) / 20 mL in 1 VIAL (71288-729-20)
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