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=ANDA201783"
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
68001-610-25 68001-610 HUMAN PRESCRIPTION DRUG Zoledronic acid Zoledronic acid INJECTION, SOLUTION, CONCENTRATE INTRAVENOUS 20240228 N/A ANDA ANDA201783 BluePoint Laboratories ZOLEDRONIC ACID 4 mg/5mL 1 VIAL, GLASS in 1 CARTON (68001-610-25) / 5 mL in 1 VIAL, GLASS
72603-198-01 72603-198 HUMAN PRESCRIPTION DRUG Zoledronic acid Zoledronic acid INJECTION, SOLUTION, CONCENTRATE INTRAVENOUS 20231101 N/A ANDA ANDA201783 NORTHSTAR RX LLC ZOLEDRONIC ACID 4 mg/5mL 1 VIAL, GLASS in 1 CARTON (72603-198-01) / 5 mL in 1 VIAL, GLASS
23155-170-31 23155-170 HUMAN PRESCRIPTION DRUG Zoledronic acid Zoledronic acid INJECTION, SOLUTION, CONCENTRATE INTRAVENOUS 20230831 N/A ANDA ANDA201783 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. ZOLEDRONIC ACID 4 mg/5mL 1 VIAL, GLASS in 1 CARTON (23155-170-31) / 5 mL in 1 VIAL, GLASS
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