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=ANDA090799"
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
63323-125-94 63323-125 HUMAN PRESCRIPTION DRUG GEMCITABINE GEMCITABINE INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20110726 N/A ANDA ANDA090799 Fresenius Kabi USA, LLC GEMCITABINE HYDROCHLORIDE 1 g/25mL 1 VIAL, SINGLE-DOSE in 1 BOX (63323-125-94) / 25 mL in 1 VIAL, SINGLE-DOSE
63323-126-03 63323-126 HUMAN PRESCRIPTION DRUG GEMCITABINE GEMCITABINE INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20110726 N/A ANDA ANDA090799 Fresenius Kabi USA, LLC GEMCITABINE HYDROCHLORIDE 2 g/50mL 1 VIAL, SINGLE-DOSE in 1 BOX (63323-126-03) / 50 mL in 1 VIAL, SINGLE-DOSE
63323-102-13 63323-102 HUMAN PRESCRIPTION DRUG GEMCITABINE GEMCITABINE INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20110726 N/A ANDA ANDA090799 Fresenius Kabi USA, LLC GEMCITABINE HYDROCHLORIDE 200 mg/5mL 1 VIAL, SINGLE-DOSE in 1 BOX (63323-102-13) / 5 mL in 1 VIAL, SINGLE-DOSE
63323-125-53 63323-125 HUMAN PRESCRIPTION DRUG GEMCITABINE GEMCITABINE INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20110726 N/A ANDA ANDA090799 Fresenius Kabi USA, LLC GEMCITABINE HYDROCHLORIDE 1 g/25mL 1 VIAL, SINGLE-DOSE in 1 BOX (63323-125-53) / 25 mL in 1 VIAL, SINGLE-DOSE
63323-102-94 63323-102 HUMAN PRESCRIPTION DRUG GEMCITABINE GEMCITABINE INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20110726 N/A ANDA ANDA090799 Fresenius Kabi USA, LLC GEMCITABINE HYDROCHLORIDE 200 mg/5mL 1 VIAL, SINGLE-DOSE in 1 BOX (63323-102-94) / 5 mL in 1 VIAL, SINGLE-DOSE
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