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=ANDA217032"
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
36000-360-10 36000-360 HUMAN PRESCRIPTION DRUG phenylephrine hydrochloride phenylephrine hydrochloride INJECTION INTRAVENOUS 20260406 N/A ANDA ANDA217032 Baxter Healthcare Corporation PHENYLEPHRINE HYDROCHLORIDE 10 mg/mL 10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (36000-360-10) / 5 mL in 1 VIAL, PHARMACY BULK PACKAGE
36000-362-05 36000-362 HUMAN PRESCRIPTION DRUG phenylephrine hydrochloride phenylephrine hydrochloride INJECTION INTRAVENOUS 20260406 N/A ANDA ANDA217032 Baxter Healthcare Corporation PHENYLEPHRINE HYDROCHLORIDE 10 mg/mL 5 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (36000-362-05) / 10 mL in 1 VIAL, PHARMACY BULK PACKAGE
36000-358-25 36000-358 HUMAN PRESCRIPTION DRUG phenylephrine hydrochloride phenylephrine hydrochloride INJECTION INTRAVENOUS 20260406 N/A ANDA ANDA217032 Baxter Healthcare Corporation PHENYLEPHRINE HYDROCHLORIDE 10 mg/mL 25 VIAL, SINGLE-DOSE in 1 CARTON (36000-358-25) / 1 mL in 1 VIAL, SINGLE-DOSE
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