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=ANDA218749"
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
70436-121-31 70436-121 HUMAN PRESCRIPTION DRUG GADOTERIDOL GADOTERIDOL INJECTION INTRAVENOUS 20250220 N/A ANDA ANDA218749 Slate Run Pharmaceuticals, LLC GADOTERIDOL 279.3 mg/mL 5 VIAL, SINGLE-DOSE in 1 CARTON (70436-121-31) / 5 mL in 1 VIAL, SINGLE-DOSE
70436-121-33 70436-121 HUMAN PRESCRIPTION DRUG GADOTERIDOL GADOTERIDOL INJECTION INTRAVENOUS 20250220 N/A ANDA ANDA218749 Slate Run Pharmaceuticals, LLC GADOTERIDOL 279.3 mg/mL 5 VIAL, SINGLE-DOSE in 1 CARTON (70436-121-33) / 10 mL in 1 VIAL, SINGLE-DOSE
70436-121-34 70436-121 HUMAN PRESCRIPTION DRUG GADOTERIDOL GADOTERIDOL INJECTION INTRAVENOUS 20250220 N/A ANDA ANDA218749 Slate Run Pharmaceuticals, LLC GADOTERIDOL 279.3 mg/mL 5 VIAL, SINGLE-DOSE in 1 CARTON (70436-121-34) / 15 mL in 1 VIAL, SINGLE-DOSE
70436-121-35 70436-121 HUMAN PRESCRIPTION DRUG GADOTERIDOL GADOTERIDOL INJECTION INTRAVENOUS 20250220 N/A ANDA ANDA218749 Slate Run Pharmaceuticals, LLC GADOTERIDOL 279.3 mg/mL 5 VIAL, SINGLE-DOSE in 1 CARTON (70436-121-35) / 20 mL in 1 VIAL, SINGLE-DOSE
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