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=NDA200795"
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
0409-0181-25 0409-0181 HUMAN PRESCRIPTION DRUG Gemcitabine GEMCITABINE INJECTION, SOLUTION INTRAVENOUS 20130709 N/A NDA NDA200795 Hospira, Inc. GEMCITABINE HYDROCHLORIDE 38 mg/mL 1 VIAL, SINGLE-DOSE in 1 CARTON (0409-0181-25) / 26.3 mL in 1 VIAL, SINGLE-DOSE
0409-0181-01 0409-0181 HUMAN PRESCRIPTION DRUG Gemcitabine GEMCITABINE INJECTION, SOLUTION INTRAVENOUS 20110826 N/A NDA NDA200795 Hospira, Inc. GEMCITABINE HYDROCHLORIDE 38 mg/mL 1 VIAL, SINGLE-DOSE in 1 CARTON (0409-0181-01) / 26.3 mL in 1 VIAL, SINGLE-DOSE
0409-0182-25 0409-0182 HUMAN PRESCRIPTION DRUG Gemcitabine GEMCITABINE INJECTION, SOLUTION INTRAVENOUS 20130729 N/A NDA NDA200795 Hospira, Inc. GEMCITABINE HYDROCHLORIDE 38 mg/mL 1 VIAL, SINGLE-DOSE in 1 CARTON (0409-0182-25) / 52.6 mL in 1 VIAL, SINGLE-DOSE
0409-0182-01 0409-0182 HUMAN PRESCRIPTION DRUG Gemcitabine GEMCITABINE INJECTION, SOLUTION INTRAVENOUS 20110822 N/A NDA NDA200795 Hospira, Inc. GEMCITABINE HYDROCHLORIDE 38 mg/mL 1 VIAL, SINGLE-DOSE in 1 CARTON (0409-0182-01) / 52.6 mL in 1 VIAL, SINGLE-DOSE
0409-0183-25 0409-0183 HUMAN PRESCRIPTION DRUG Gemcitabine GEMCITABINE INJECTION, SOLUTION INTRAVENOUS 20130709 N/A NDA NDA200795 Hospira, Inc. GEMCITABINE HYDROCHLORIDE 38 mg/mL 1 VIAL, SINGLE-DOSE in 1 CARTON (0409-0183-25) / 5.26 mL in 1 VIAL, SINGLE-DOSE
0409-0183-01 0409-0183 HUMAN PRESCRIPTION DRUG Gemcitabine GEMCITABINE INJECTION, SOLUTION INTRAVENOUS 20110824 N/A NDA NDA200795 Hospira, Inc. GEMCITABINE HYDROCHLORIDE 38 mg/mL 1 VIAL, SINGLE-DOSE in 1 CARTON (0409-0183-01) / 5.26 mL in 1 VIAL, SINGLE-DOSE
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