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=ANDA218256"
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
60219-2550-1 60219-2550 HUMAN PRESCRIPTION DRUG prednisolone acetate prednisolone acetate SUSPENSION/ DROPS OPHTHALMIC 20250613 N/A ANDA ANDA218256 Amneal Pharmaceuticals NY LLC PREDNISOLONE ACETATE 10 mg/mL 1 BOTTLE, PLASTIC in 1 CARTON (60219-2550-1) / 5 mL in 1 BOTTLE, PLASTIC
60219-2552-1 60219-2552 HUMAN PRESCRIPTION DRUG prednisolone acetate prednisolone acetate SUSPENSION/ DROPS OPHTHALMIC 20250613 N/A ANDA ANDA218256 Amneal Pharmaceuticals NY LLC PREDNISOLONE ACETATE 10 mg/mL 1 BOTTLE, PLASTIC in 1 CARTON (60219-2552-1) / 15 mL in 1 BOTTLE, PLASTIC
60219-2551-1 60219-2551 HUMAN PRESCRIPTION DRUG prednisolone acetate prednisolone acetate SUSPENSION/ DROPS OPHTHALMIC 20250613 N/A ANDA ANDA218256 Amneal Pharmaceuticals NY LLC PREDNISOLONE ACETATE 10 mg/mL 1 BOTTLE, PLASTIC in 1 CARTON (60219-2551-1) / 10 mL in 1 BOTTLE, PLASTIC
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