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=ANDA209077"
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
25021-239-52 25021-239 HUMAN PRESCRIPTION DRUG Gemcitabine gemcitabine INJECTION, SOLUTION INTRAVENOUS 20190115 N/A ANDA ANDA209077 Sagent Pharmaceuticals GEMCITABINE HYDROCHLORIDE 38 mg/mL 1 VIAL in 1 CARTON (25021-239-52) / 52.6 mL in 1 VIAL
25021-239-26 25021-239 HUMAN PRESCRIPTION DRUG Gemcitabine gemcitabine INJECTION, SOLUTION INTRAVENOUS 20190115 N/A ANDA ANDA209077 Sagent Pharmaceuticals GEMCITABINE HYDROCHLORIDE 38 mg/mL 1 VIAL in 1 CARTON (25021-239-26) / 26.3 mL in 1 VIAL
25021-239-05 25021-239 HUMAN PRESCRIPTION DRUG Gemcitabine gemcitabine INJECTION, SOLUTION INTRAVENOUS 20190115 N/A ANDA ANDA209077 Sagent Pharmaceuticals GEMCITABINE HYDROCHLORIDE 38 mg/mL 1 VIAL in 1 CARTON (25021-239-05) / 5.26 mL in 1 VIAL
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