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=ANDA210383"
符合检索条件的记录共 3 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
50742-498-05 50742-498 HUMAN PRESCRIPTION DRUG GEMCITABINE gemcitabine INJECTION, SOLUTION INTRAVENOUS 20230701 N/A ANDA ANDA210383 Ingenus Pharmaceuticals, LLC GEMCITABINE HYDROCHLORIDE 38 mg/mL 1 VIAL, SINGLE-DOSE in 1 CARTON (50742-498-05) / 5.26 mL in 1 VIAL, SINGLE-DOSE
50742-497-53 50742-497 HUMAN PRESCRIPTION DRUG GEMCITABINE gemcitabine INJECTION, SOLUTION INTRAVENOUS 20230701 N/A ANDA ANDA210383 Ingenus Pharmaceuticals, LLC GEMCITABINE HYDROCHLORIDE 38 mg/mL 1 VIAL, SINGLE-DOSE in 1 CARTON (50742-497-53) / 52.6 mL in 1 VIAL, SINGLE-DOSE
50742-496-26 50742-496 HUMAN PRESCRIPTION DRUG GEMCITABINE gemcitabine INJECTION, SOLUTION INTRAVENOUS 20230701 N/A ANDA ANDA210383 Ingenus Pharmaceuticals, LLC GEMCITABINE HYDROCHLORIDE 38 mg/mL 1 VIAL, SINGLE-DOSE in 1 CARTON (50742-496-26) / 26.3 mL in 1 VIAL, SINGLE-DOSE
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