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=ANDA207310"
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
63323-623-76 63323-623 HUMAN PRESCRIPTION DRUG Sodium chloride SODIUM CHLORIDE INJECTION, SOLUTION INTRAVENOUS 20170919 N/A ANDA ANDA207310 Fresenius Kabi USA, LLC SODIUM CHLORIDE 9 mg/mL 1000 mL in 1 BAG (63323-623-76)
17271-701-02 17271-701 HUMAN PRESCRIPTION DRUG Sodium chloride SODIUM CHLORIDE INJECTION, SOLUTION INTRAVENOUS 20170919 N/A ANDA ANDA207310 Becton Dickinson and Company SODIUM CHLORIDE 9 mg/mL 50 mL in 1 BAG (17271-701-02)
17271-701-03 17271-701 HUMAN PRESCRIPTION DRUG Sodium chloride SODIUM CHLORIDE INJECTION, SOLUTION INTRAVENOUS 20170919 N/A ANDA ANDA207310 Becton Dickinson and Company SODIUM CHLORIDE 9 mg/mL 100 mL in 1 BAG (17271-701-03)
17271-701-05 17271-701 HUMAN PRESCRIPTION DRUG Sodium chloride SODIUM CHLORIDE INJECTION, SOLUTION INTRAVENOUS 20170919 N/A ANDA ANDA207310 Becton Dickinson and Company SODIUM CHLORIDE 9 mg/mL 250 mL in 1 BAG (17271-701-05)
17271-701-06 17271-701 HUMAN PRESCRIPTION DRUG Sodium chloride SODIUM CHLORIDE INJECTION, SOLUTION INTRAVENOUS 20170919 N/A ANDA ANDA207310 Becton Dickinson and Company SODIUM CHLORIDE 9 mg/mL 500 mL in 1 BAG (17271-701-06)
17271-701-07 17271-701 HUMAN PRESCRIPTION DRUG Sodium chloride SODIUM CHLORIDE INJECTION, SOLUTION INTRAVENOUS 20170919 N/A ANDA ANDA207310 Becton Dickinson and Company SODIUM CHLORIDE 9 mg/mL 1000 mL in 1 BAG (17271-701-07)
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