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=NDA016269"
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
51662-1468-1 51662-1468 HUMAN PRESCRIPTION DRUG MANNITOL MANNITOL INJECTION, SOLUTION INTRAVENOUS 20191213 N/A NDA NDA016269 HF Acquisition Co LLC, DBA HealthFirst MANNITOL 12.5 g/50mL 50 mL in 1 VIAL, SINGLE-DOSE (51662-1468-1)
51662-1468-3 51662-1468 HUMAN PRESCRIPTION DRUG MANNITOL MANNITOL INJECTION, SOLUTION INTRAVENOUS 20221211 N/A NDA NDA016269 HF Acquisition Co LLC, DBA HealthFirst MANNITOL 12.5 g/50mL 25 POUCH in 1 CASE (51662-1468-3) / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1468-2) / 50 mL in 1 VIAL, SINGLE-DOSE
0404-9905-50 0404-9905 HUMAN PRESCRIPTION DRUG Mannitol Mannitol INJECTION, SOLUTION INTRAVENOUS 20220112 N/A NDA NDA016269 Henry Schein, Inc. MANNITOL 12.5 g/50mL 1 VIAL, SINGLE-DOSE in 1 BAG (0404-9905-50) / 50 mL in 1 VIAL, SINGLE-DOSE
0409-4031-01 0409-4031 HUMAN PRESCRIPTION DRUG Mannitol MANNITOL INJECTION, SOLUTION INTRAVENOUS 20041130 N/A NDA NDA016269 Hospira, Inc. MANNITOL 12.5 g/50mL 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4031-01) / 50 mL in 1 VIAL, SINGLE-DOSE (0409-4031-16)
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